Prostacyclin compounds, compositions and methods of use thereof

ABSTRACT

Prostacyclin compounds and compositions comprising the same are provided herein. Specifically, prostacyclin compounds comprising treprostinil covalently linked to a linear C 5 -C 18  alkyl, branched C 5 -C 18  alkyl, linear C 2 -C 18  alkenyl, branched C 3 -C 18  alkenyl, aryl, aryl-C 1 -C 18  alkyl or an amino acid or a peptide (e.g., dipeptide, tripeptide, tetrapeptide) are described. The linkage, in one embodiment, is via a carbamate, amide or ester bond. Prostacyclin compounds provided herein can also include at least one hydrogen atom substituted with at least one deuterium atom. Methods for treating pulmonary hypertension (e.g., pulmonary arterial hypertension) and portopulmonary hypertension are also provided.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority from U.S. Provisional Application Ser. Nos. 62/042,123, filed Aug. 26, 2014; 62/028,758, filed Jul. 24, 2014; 61/950,967, filed Mar. 11, 2014; 61/910,703, filed Dec. 2, 2013; 61/895,680, filed Oct. 25, 2013; each of which is incorporated by reference in its entirety for all purposes.

BACKGROUND OF THE INVENTION

Pulmonary hypertension (PH) is characterized by an abnormally high blood pressure in the lung vasculature. It is a progressive, lethal disease that leads to heart failure and can occur in the pulmonary artery, pulmonary vein, or pulmonary capillaries. Symptomatically patients experience shortness of breath, dizziness, fainting, and other symptoms, all of which are made worse by exertion. There are multiple causes, and can be of unknown origin, idiopathic, and can lead to hypertension in other systems, for example, portopulmonary hypertension in which patients have both portal and pulmonary hypertension.

Pulmonary hypertension has been classified into five groups by the World Health Organization (WHO). Group I is called pulmonary arterial hypertension (PAH ), and includes PAH that has no known cause (idiopathic), inherited PAH (i.e., familial PAH or FPAH), PAH that is caused by drugs or toxins, and PAH caused by conditions such as connective tissue diseases, HIV infection, liver disease, and congenital heart disease. Group II pulmonary hypertension is characterized as pulmonary hypertension associated with left heart disease. Group III pulmonary hypertension is characterized as PH associated with lung diseases, such as chronic obstructive pulmonary disease and interstitial lung diseases, as well as PH associated with sleep-related breathing disorders (e.g., sleep apnea). Group IV PH is PH due to chronic thrombotic and/or embolic disease, e.g., PH caused by blood clots in the lungs or blood clotting disorders. Group V includes PH caused by other disorders or conditions, e.g., blood disorders (e.g., polycythemia vera, essential thrombocythemia), systemic disorders (e.g., sarcoidosis, vasculitis), metabolic disorders (e.g., thyroid disease, glycogen storage disease).

Pulmonary arterial hypertension (PAH) afflicts approximately 200,000 people globally with approximately 30,000-40,000 of those patients in the United States. PAH patients experience constriction of pulmonary arteries which leads to high pulmonary arterial pressures, making it difficult for the heart to pump blood to the lungs. Patients suffer from shortness of breath and fatigue which often severely limits the ability to perform physical activity.

The New York Heart Association (NYHA) has categorized PAH patients into four functional classes, used to rate the severity of the disease. Class I PAH patients as categorized by the NYHA, do not have a limitation of physical activity, as ordinary physical activity does not cause undue dyspnoea or fatigue, chest pain, or near syncope. Treatment is not needed for class I PAH patients. Class II PAH patients as categorized by the NYHA have a slight limitation on physical activity. These patients are comfortable at rest, but ordinary physical activity causes undue dyspnoea or fatigue, chest pain or near syncope. Class III PAH patients as categorized by the NYHA have a marked limitation of physical activity. Although comfortable at rest, class III PAH patients experience undue dyspnoea or fatigue, chest pain or near syncope as a result of less than ordinary physical activity. Class IV PAH patients as categorized by the NYHA are unable to carry out any physical activity without symptoms. Class IV PAH patients might experience dyspnoea and/or fatigue at rest, and discomfort is increased by any physical activity. Signs of right heart failure are often manifested by class IV PAH patients,

Patients with PAH are treated with an endothelin receptor antagonist (ERA), phosphodiesterase type 5 (PDE-5) inhibitor, a guanylate cyclase stimulator, a prostanoid (e.g., prostacyclin), or a combination thereof. ERAs include abrisentan (Letairis®), sitaxentan, bosentan (Tracleer®), and macitentan (Opsumit®). PDE-5 inhibitors indicated for the treatment of PAH include sildenafil (Revatio®), tadalafil (Adcirca®). Prostanoids indicated for the treatment of PAH include iloprost, epoprosentol and treprostinil (Remodulin®, Tyvaso®). The one approved guanylate cyclase stimulator is riociguat (Adempas®. Additionally, patients are often treated with combinations of the aforementioned compounds.

Portopulmonary hypertension is defined by the coexistence of portal and pulmonary hypertension, and is a serious complication of liver disease. The diagnosis of portopulmonary hypertension is based on hemodynamic criteria: (1) portal hypertension and/or liver disease (clinical diagnosis-ascites/varices/splenomegaly), (2) mean pulmonary artery pressure >25 mmHg at rest, (3) pulmonary vascular resistance >240 dynes s/enr, (4) pulmonary artery occlusion pressure <15 mmHg or transpulmonary gradient >12 mmHg. PPH is a serious complication of liver disease, and is present in 0.25 to 4% of patients suffering from cirrhosis. Today, PPH is comorbid in 4-6% of those referred for a liver transplant.

Despite there being treatments for PAH and PPH, the current prostacyclin therapies are associated with severe toxicity and tolerability issues, as well as the requirement for inconvenient dosing schedules. The present invention overcomes addresses these factors by providing compounds and treatment schedules that provide for less toxicity, better tolerability and more convenient dosing schedules.

SUMMARY OF THE INVENTION

In one aspect of the invention, a prostacyclin compound of Formula (I), or a pharmaceutically acceptable salt, is provided:

wherein R₁ is NH, O or S; R₂ is H, a linear C₅-C₁₈ alkyl, branched C₅-C₁₈ alkyl, linear C₂-C₁₈ alkenyl, branched C₃-C₁₈ alkenyl, aryl; aryl-C₁-C₁₈ alkyl; an amino acid or a peptide; R₃ is H, OH, O-alkyl or O-alkenyl; R₄ is an optionally substituted linear or branched C₁-C₁₅ alkyl, or an optionally substituted linear or branched C₂-C₁₅ alkenyl; and n is an integer from 0 to 5, with the proviso that the prostacyclin compound is not treprostinil.

In another aspect of the invention, a prostacyclin compound of Formula (II), or a pharmaceutically acceptable salt, is provided:

wherein R₁ is NH, O or S; R₂ is a linear or branched C₅-C₁₈ alkyl, a linear C₂-C₁₈ alkenyl or a branched C₃-C₁₈ alkenyl, aryl, aryl-C₁-C₁₈ alkyl, an amino acid or a peptide; and n is an integer from 0 to 5.

In one embodiment, a compound of Formula (I) and/or (II) is provided, wherein one or more hydrogen atoms is substituted with a deuterium. Accordingly, in one embodiment, the present invention relates to an isotopologue of Formula (I) and/or (II), substituted with one or more deuterium atoms. The isotopologue of Formula (I) and/or (II) may be used to accurately determine the concentration of compounds of Formula (I) and/or (II) in biological fluids and to determine metabolic patterns of compounds of Formula (I) and/or (II) and its isotopologues. The invention further provides compositions comprising these deuterated isotopologues and methods of treating diseases and conditions, as set forth herein.

In one embodiment of the invention, a compound of Formula (I) or (II), or a pharmaceutical ly acceptable salt, is provided, wherein R₁ is N and n is 1. In a further embodiment, R₂ is a linear C₅-C₁₈ alkyl or a branched C₅-C₁₈ alkyl. In a further embodiment, R₂ is a linear C₆-C₁₂ alkyl or a branched C₆-C₁₂ alkyl.

Another embodiment of the invention provides a compound of Formula (I) or (II), wherein R₁ is O and n is 1. In another embodiment, a compound of Formula (I) or (II) is provided, wherein R₁ is S and n is 1. In yet another embodiment of the invention, a compound of Formula (I) or (II) is provided, wherein R₁ is N and n is 0.

Another embodiment of the invention provides a prostacyclin compound of Formula (I) or (II), wherein R₂ is a linear C₅-C₁₈ alkyl. In a further embodiment, n is 0 or 1. In even a further embodiment, R₁ is N or O. In yet a further embodiment, R₂ is a linear C₆-C₁₆ alkyl. Yet another embodiment provides a prostacyclin compound of Formula (I) or (II), wherein R₁ is N, R₂ is a linear C₆-C₁₈ alkyl, and n is 1. In even a further embodiment, R₂ is a linear C₆, C₈ C₁₀, C₁₂, or C₁₄ alkyl.

Another embodiment of the invention provides a prostacyclin compound of Formula (I) or (II), or a pharmaceutically acceptable salt, wherein R₂ is a branched C₅-C₁₈ alkyl. In a further embodiment, n is 0 or 1. In yet a further embodiment, R₁ is N or O. In even a further embodiment, the branched alkyl is hexyl, octyl, decyl, dodecyl, tetradecyl, hexadecyl or octadecyl.

In yet another embodiment, a prostacyclin compound of Formula (I) or (II), or a pharmaceutically acceptable salt, is provided, wherein R₂ is a linear C₅-C₁₈ alkenyl. In a further embodiment, n is 0 or 1. In yet a further embodiment, R₁ is N or O. In even a further embodiment, the branched alkyl is hexyl, octyl, decyl, dodecyl, tetradecyl, hexadecyl or octadecyl.

In yet another embodiment, a prostacyclin compound of Formula (I) or (II), or a pharmaceutically acceptable salt, is provided, wherein R₂ is a branched C₅-C₁₈ alkenyl, In a further embodiment, n is 0 or 1. In yet a further embodiment, R₁ is N or O. In yet a further embodiment, the branched alkenyl is pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl or octadecenyl.

In one embodiment, a prostacyclin compound of Formula (I) or (II), or a pharmaceutically acceptable salt, is provided, wherein R₂ is a branched chain alkyl that is either a symmetrical branched alkyl or an asymmetrical branched alkyl. In one embodiment of Formula (I) or (II), R₁ is O or N and R₂ is

where m1 and m2 are independently an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl. When m1 and/or m2 is an integer from 2-9, the m1/m2 at the end of the carbon chain is CH₃, while the remaining m1/m2 groups are CH₂. In a further embodiment, n is 0 or 1. In even a further embodiment, n is 1, R₁ is O, R₂ is

and the following compound is provided:

or a pharmaceutically acceptable salt thereof. In one embodiment, m1 and m2 are both 4. In another embodiment, m1 is 3 and m2 is 4. In even a further embodiment, n is 1.

In one embodiment, a compound of Formula (I) or (II) is provided, R₁ is O and R is

In yet another embodiment of Formula (I) or (II), R₁ is O and R₂ is

In one embodiment, a compound of Formula (I) or (II) is provided, R₁ is N and R₂ is

In yet another embodiment of Formula (I) or (II), R₁ is N and R₂ is

In a further embodiment, n is 1 and the following compound is provided:

In one embodiment, the prostacyclin compounds of the formulae provided herein having a branched alkyl or branched alkenyl (e.g., where R₂ of the formulae provided herein is 5-nonanyl, 3-heptyl, 4-heptyl, 4-octyl, 3-octyl, 2-octyl, 2-dimethyl-1-propyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, 3-pentyl) at position R₂ exhibit a slower conversion rate relative to a prostacyclin compound having a linear alcohol chain at position R₂, and have the further advantage of high solubility.

Yet another embodiment of the invention relates to a prostacyclin compound of Formula (III), or a pharmaceutically acceptable salt:

wherein R₁ and R₂ are defined above, and

R₅ and R₆ are independently selected from H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₂-C₁₅ alkenyl, (C═O)— optionally substituted linear or branched C₁-C₃₅ alkyl, or (C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl, with the proviso that the prostacyclin compound of Formula (HI) is not treprostinil.

Another aspect of the invention relates to a prostacyclin composition comprising a prostacyclin compound of Formula (I), (II) or (III). In one embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (II) or (III) and a hydrophobic additive. In a further embodiment, the hydrophobic additive is a hydrocarbon, a terpene or a hydrophobic lipid. In another embodiment, the hydrophobic additive is eholesteryl acetate, ethyl stearate, palmitate, myristate, palmityl palmitate, tocopheryl acetate, a monoglyceride, a diglyceri.de, a triglyceride like palmitate, myristate, dodecanoate, decanoate, octanoate or squalane. In even a further embodiment, the hydrophobic additive is squalane.

In another aspect of the invention, a composition comprising a prostacyclin compound of Formula (I), (II) or (III), and an amphiphilic agent is provided. In one embodiment, the amphiphilic agent is a PEGylated lipid, a surfactant or a block copolymer. In a further embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (II) or (III), and a PEGylated lipid. In a further embodiment, the PEGylated lipid comprises PEG400, PEG500, PEG1000, PEG2000, PEG3000, PEG4000, or PEG5000. In a further embodiment the lipid component of the PEGylated lipid comprises PEG covalently linked to dimyristoyl phosphatidylethanolamine (DMPE), dipalmitoyl phosphoethanolamine (DPPE), distearoylphosphatidylethanolamine (DSPE), dimyristoylglycerol glycerol (DMG), diphosphatidylglycerol (DPG), disteraroylglycerol (DSG).

In another embodiment of the invention, a composition comprising a prostacyclin compound of Formula. (I), (II) or (III), a hydrophobic additive and an amphiphilic agent is provided. In one embodiment, the amphiphilic agent is a PEGylated lipid, a surfactant or a block copolymer. In a further embodiment, the hydrophobic additive is squalane. In a further embodiment, a PEGylated lipid is present in the composition and comprises PEG400, PEG500, PEG1000, PEG2000, PEG3000, PEG4000 or PEG5000.

In another aspect of the invention, a method for treating pulmonary hypertension (PH) is provided . The treatment methods include treatment of group I (PAH), group II, group III, group IV or group V PH. In one embodiment, the method for treating PH comprises treatment of pulmonary arterial hypertension (PAH) in a patient in need thereof. In one embodiment, the method for treating PAH comprises administering to the patient in need of treatment, a prostacyclin compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof, or a composition comprising a prostacyclin compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof,. In a further embodiment, the administration is subcutaneous, oral, nasal, intravenous or a pulmonary route of administration. In the case of pulmonary administration, the compound of Formula (I), (II) or (III), or the composition comprising the prostacyclin compound of Formula (I), (II) or (III) is administered to the patient via a nebulizer, dry powder inhaler, or metered dose inhaler.

In another aspect of the invention, a method for treating portopulmonary hypertension (PPH) in a patient in need thereof is provided. In one embodiment, the method for treating PPH comprises administering to the patient in need of treatment, a prostacyclin compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof, or a composition comprising a prostacyclin compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof,. In a further embodiment, the administration is subcutaneous, oral, nasal, intravenous or a pulmonary route of administration. In the case of pulmonary administration, the compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof, or the composition comprising the prostacyclin compound of Formula (I), (II) or (III) is administered to the patient via a nebulizer, dry powder inhaler, or metered dose inhaler.

In one embodiment of the invention, a method for treating PH, PAH or PPH in a patient in need thereof is provided, comprises administering to the lungs of the patient a prostacyclin compound of Formula (I), (II) or (III), or a pharmaceutically acceptable salt thereof, via a metered dose inhaler comprising a propellant. In a further embodiment, the propellant is a fluorocarbon. In one embodiment, the compound of Formula (I), (II) or (III) or pharmaceutically acceptable salt thereof is administered via a metered dose inhaler to the lungs of a patient in need of PH, PAH or PPH treatment, and administration occurs once, twice or three times daily. In embodiments where the compound of Formula (I), (II) or (III), or a composition comprising the compound of Formula (I), (II) or (III), is administered orally, nasally, subcutaneously, intravenously or to the lungs (e.g., via nebulization, dry powder inhaler or metered dose inhaler), administration to the patient is either once or twice daily. In one embodiment, the compound of Formula (I), (II) or (III), or a composition comprising the compound of Formula (I), (II) or (III) is administered once daily to the patient in need of treatment, and administration is subcutaneous, intravenous, oral, nasal, or to the lungs via aerosolization using a nebulizer, dry powder inhaler, or metered dose inhaler.

In one embodiment, the patient treated for PH, PAH or PPH with the compounds, compositions and methods described herein experiences a decreased number of side effect(s), or a reduction in severity of side effect(s), compared to the number of side effect(s) or severity of side effect(s) experienced when the patient is administered treprostinil. In one embodiment, the side effect is the patient's cough response, and the frequency and/or severity is reduced, as compared to the frequency and/or severity of cough response experienced by the patient when administered treprostinil.

In another embodiment, the prostacyclin compound administered to a patient in need thereof via a pulmonary route by the PH, PAH or PPH treatment methods described herein provides a greater pulmonary elimination half-life (t_(1/2)) of the prostacyclin compound and/or its metabolite treprostinil, compared to the pulmonary elimination half-life (t_(1/2)) of treprostinil, when treprostinil is administered via a pulmonary route (e.g., by nebulization, dry powder inhaler, or a metered dose inhaler) to the patient.

In another embodiment, the prostacyclin compound administered to a patient in need thereof, via the PH, PAH or PPH treatment methods described herein provides a greater systemic half-life (t_(1/2)) of the prostacyclin compound and/or its metabolite treprostinil, compared to the systemic elimination half-life (t_(1/2)) of treprostinil, when treprostinil is administered to the patient. In a further embodiment, administration of the prostacyclin compound and treprostinil comprises subcutaneous or intravenous administration.

In another embodiment, the prostacyclin compound administered to a patient in need of PH, PAH or PPH treatment provides a greater mean pulmonary C_(max) and/or lower plasma C_(max) of treprostinil for the patient, compared to the respective pulmonary or plasma C_(max) of treprostinil, when treprostinil is administered to the patient.

In another embodiment, the prostacyclin compound administered to a patient in need of PH (e.g., PAH) or PPH treatment provides a greater mean pulmonary or plasma area under the curve (AUC_(0-t)) of the prostacyclin compound and/or its metabolite treprostinil, compared to the mean pulmonary or plasma area under the curve (AUC_(0-t)) of treprostinil, when treprostinil is administered to the patient. In yet another embodiment, the prostacyclin compound administered to a patient in need thereof provides a greater pulmonary or plasma time to peak concentration (t_(max)) of the prostacyclin compound and/or its metabolite treprostinil, compared to the pulmonary or plasma time to peak concentration (tmax) of treprostinil, when treprostinil is administered to the patient.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A is a graph showing the spontaneous hydrolysis of treprostinil compounds vs. time. (C3: propyl ester, C4: butyl ester, C5: pentyl ester, C6: hexyl ester, C8: octyl ester and C10: decyl ester).

FIG. 1B is a graph showing esterase-mediated hydrolysis of the alkyl chains at various timepoints (15 min., 30 min,, 60 min.) of treprostinil compounds dissolved in aqueous buffer, and treprostinil compositions comprising PEGylated lipids.

FIG. 2 is a graph of the average particle diameter for various treprostinil alkyl esters in formulations comprising PEGylated lipids as a function of alkyl ester chain length. The alkyl chain is present at the carboxylic acid moiety of treprostinil. PD is polydispersity.

FIGS. 3A, 3B and 3C are graphs of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. time, in response to 10 μM (FIG. 3A), 1 μM (FIG. 3B) or 0.1 μM (FIG. 3C) treprostinil and treprostinil alkyl ester compositions. (C6: hexyl ester, C8: octyl ester, C10: decyl ester).

FIG. 4 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. time, in response to 5 μM treprostinil and treprostinil alkyl ester compositions. (C6: hexyl ester, C8: octyl ester, C10: decyl ester, C12: dodecyl ester).

FIG. 5 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. time, in response to challenge with treprostinil and various treprostinil alkyl ester compounds at 5 μM.

FIG. 6 is graph of relative cAMP activity of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. time, in response to challenge with treprostinil and nebulized and non-nebulized treprostinil alkyl ester compositions, as measured by a modified GloSensor assay. “(N)” indicates nebulized compositions.

FIG. 7 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. free treprostinil, at various dosages and time points.

FIG. 8 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. T554 (C₂-TR) treprostinil alkyl ester composition challenge, at various dosages and time points.

FIG. 9 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. T568 (C₁₂-TR) treprostinil alkyl ester composition challenge, at various dosages and time points.

FIG. 10 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. T631 (C₁₄-TR) treprostinil alkyl ester composition challenge, at various dosages and time points.

FIG. 11 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. T623 (C₁₆-TR) treprostinil alkyl ester composition challenge, at various dosages and time points.

FIG. 12 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. treprostinil ethyl ester (C₂)) compound challenge, at various dosages and time points.

FIG. 13 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. treprostinil ethyl ester (C₁₂) compound challenge, at various dosages and time points.

FIG. 14 is a graph of relative cAMP response of CHO—K1-P4 cells (2.5×10⁴ cells/well) vs. treprostinil ethyl ester (C₂) compositions, at various dosages and time points.

FIG. 15A is a graph of pulmonary arterial pressure (expressed as a percent of the starting hypoxia value) vs. time, in response to animal challenge with phosphate buffered saline (PBS), treprostinil, and prostacyclin compositions (T554 (C₂) and T-568 (C₁₂)). The target dose for treprostinil and prostacyclin alkyl esters was 76.8 nmole/kg; the achieved deposited dose may be 5× lower than these target values.

FIG. 15B is a dot plot showing the effect of treprostinil and C₂, C₈, C₁₀, and C₁₂ treprostinil alkyl ester compositions on PAP (expressed as a percent of the starting hypoxia value) in an in vivo acute hypoxia rat model of PAH. Doses were target values and actual achieved lung doses may be approximately 5× lower.

FIG. 16 is a graph of systemic arterial pressure (expressed as a percent of the starting hypoxia value) vs. time, in response to animal challenge with PBS, treprostinil, and treprostinil alkyl ester compositions (T554 (C₂-TR) and T-568 (C₁₂-TR)) in an in vivo acute hypoxia rat model of PAH. The vertical dotted line marks change in x-axis time increments. The target dose for treprostlnil and prostacyclin alkyl esters was 76.8 nmole/kg; the achieved deposited dose may be 5× lower than these target values.

FIG. 17 is a graph of in vivo heart rate (expressed as a percent of the starting hypoxia value) vs. time, in response to animal challenge with PBS, treprostinil and treprostlnil alkyl ester compositions (T554 (C₂) and T-568 (C₁₂)) in an in vivo acute hypoxia rat model of PAH. The vertical dashed line marks change in x-axis time increments. The target dose for treprostinil and prostacyclin alkyl esters was 76.8 nmole/kg; the achieved deposited dose may be 5× lower than these target values.

FIG. 18, top panel, is a graph of relative cAMP response of CHO—K1 cells as a function of 5C9-TR (5-nonanyl-treprostini.l alkyl ester composition) challenge, at various dosages and time points. FIG. 18, bottom panel, shows the EC₅₀ of 5C₉-TR over time, calculated from the cAMP response of CHO—K1 cells vs. 5C9-TR.

FIG. 19, top panel, is a graph of relative cAMP response of CHO—K1 cells vs. C₁₄-TR (C₁₄ treprostinil alkyl ester composition) challenge, at various dosages and time points. FIG. 19, bottom panel, shows the EC₅₀ of C₁₄-TR over time, calculated from the cAMP response of CHO—K1 cells vs. C₁₄-TR.

FIG. 20, top panel, is a graph of relative cAMP response of CHO—K1 cells vs. C₁₆-TR (Cis treprostlnil alkyl ester composition) challenge, at various dosages and time points. FIG. 20, bottom panel, shows the EC₅₀ of C₁₄-TR over time, calculated from the cAMP response ofCHQ-K1 cells vs. C₁₄-TR.

FIG. 21 are graphs of relative cAMP response of CHO—K1 cells vs. time, in response to challenge with C₁₂-TR, C₁₄-TR, C₁₆-TR, or 5-nonanyl-TR (5C₉-TR) at 10 μM (top panel) or 5 μM (bottom panel).

FIG. 22 (top panel) is a graph of relative cAMP response of CHO—K1 cells vs. T679 (C-₁₄-TR 45 mol %, squalane 45 mol %, chol-PEG2k 10%) treprostlnil alkyl ester composition challenge, at various dosages and time points. FIG. 22 (bottom panel) shows the EC₅₀ of T679 over time, calculated from the cAMP response of CHO—K1 cells vs. T679.

FIG. 23 is a graph of relative cAMP response of CHO—K1 cells vs. time, in response to challenge with treprostinil, T631 (C₁₄-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), or T679 (C₁₄-TR 45 mol %, squalane 45 mol %, chol-PEG2k 10 mol %) at 10 μM (top panel) or 5 μM (bottom panel).

FIG. 24, top panel, is a graph of relative cAMP response of CHO—K1 cells vs. T647 (C₁₄-TR 90 mol %, cholPEG2k 10 mol %) treprostinil alkyl ester composition challenge, at various dosages and time points. FIG. 24, bottom panel, shows the EC50 of T647 over time, calculated from the cAMP responses of CHO—K1 cells v. T647-TR.

FIG. 25 are graphs of relative cAMP response of CHO—K1 cells vs. time, in response to challenge with treprostinil, T631 (C₁₄-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), or T647 (C₁₄-TR 90 mol %, chol-PEG2k 10 mol %) at 10 μM (fop panel) or 5 μM (bottom panel).

FIG. 26, top panel, is a graph of relative cAMP responses of CHO—K1 cells v. T637 (C₁₈-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %) treprostinil alkyl ester lipid nanoparticle composition challenge, at various dosages and time points. FIG. 26, bottom panel, shows the EC50 of T637 over time, calculated from the cAMP responses of CHO—K1 cells v. T637-TR.

FIG. 27 are graphs of relative cAMP response of CHO—K1 cells vs. time, in response to challenge with treprostinil, T555 (C₈-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), T556 (C₁₀-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), T568 (C₁₂-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), T631 (C₁₄-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), T623 (C₁₆-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), or T637 (C₁₈-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %) at 10 μM (top panel) or 5 μM (bottom panel).

FIG. 28 is a graph of the conversion rate (% of total) over time (hours) for linear (C₈TR) versus branched (2-dimethyl-1-propanyl-TR, 3,3-dimethyl-1-butanyl-TR, 2-ethyl-1-butanyl-TR, 5-nonanyl-TR, or 3-pentanyl-TR) prostacyclin compounds.

FIG. 29 is a graph showing the conversion of treprostinil compounds derivatized with various linear alkyl chains, relative to the conversion of the treprostinil compound derivatized with an octyl moiety (R₂═C₈). Conversion was measured at 1 hr after incubation with esterase.

FIG. 30 is a graph showing the conversion of treprostinil compounds derivatized with various branched alkyl chains, relative to the conversion of the treprostinil compound derivatized with an octyl moiety (R₂═C₈). Conversion was measured at 1 hr after incubation with esterase.

FIG. 31 is a schematic of the Jaeger-NYU nose only directed-flow inhalation exposure system (CH Technologies, Westwood, NJ, www.onares.org) used for a 24-hour pharmacokinetics study.

FIG. 32, left, is a graph of treprostinil blood plasma levels (ng/mL) as a function of time for treprostinil and various inhaled treprostinil alkyl ester formulations. FIG. 32, right, is a graph of treprostinil blood plasma levels (ng/mL) as a function of time for treprostinil and various inhaled treprostinil alkyl ester micelle formulations.

FIG. 33 is a graph of treprostinil and treprostinil alkyl ester concentration in the lung after dosing with nebulized treprostinil solution or formulated treprostinil alkyl ester suspensions. Lungs were collected at 6 hours after dosing. Treprostinil alkyl ester concentration is presented as treprostinil equivalent on a mole base.

FIG. 34, top, is a graph of treprostinil blood plasma levels (ng/mL) as a function of time in rats after nose-only inhalation of nebulized treprostinil alkyl ester formulations. FIG. 34, bottom, is a graph of treprostinil and treprostinil alkyl ester blood plasma levels (ng/mL) as a function of time in rats after nose-only inhalation of nebulized treprostinil alkyl ester formulations.

FIG. 35, top is a graph of treprostinil blood plasma levels (ng/mL) as a function of time after nebulization of various concentrations of C₁₆-TR formulations (nose only dosing). FIG. 35, bottom is a graph of treprostinil and C₁₆-TR blood plasma levels (ng/mL) as a function of time after nebulization of various concentrations of C₁₆-TR formulations (nose only dosing).

FIG. 36 is a graph of plasma concentrations of treprostinil (ng/mL) in intubated dogs as a function of time, after administration of treprostinil or the T623 lipid nanopardcle formulation (C₁₆-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %).

FIG. 37, left is a graph of treprostinil alkyl ester conversion to treprostinil as function of time for various treprostinil alkyl esters exposed to rat lung tissue homogenate. FIG. 37, right, is a graph of C₁₂-treprostinil conversion to treprostinil as function of time in rat, dog and monkey lung tissue homogenate.

FIG. 38 is a graph of mean pulmonary arterial pressure (mPAP) as a function of time in rats treated with PBS, treprostinil, T568 (C₁₂-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %) or T623 (C₁₆-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %).

FIG. 39 top, is a graph of mean systemic arterial pressure (mSAP) as a function of time in rats treated with PBS, treprostinil, T568 or T623. FIG. 39, bottom, is a graph of heart rate as a function of time in rats treated with PBS, treprostinil, T568 or T623.

FIG. 40 is a graph of treprostini l blood plasma levels (ng/mL) as a function of time in rats after administration of free treprostinil, T568 or T623.

FIG. 41 is a graph of treprostinil blood plasma levels (ng/mL) as a function of time in rats after administration of composition T763 i

DETAILED DESCRIPTION OF THE INVENTION

The term “alkyl” as used herein refers to both a straight chain alkyl, wherein alkyl chain length is indicated by a range of numbers, and a branched alkyl, wherein a branching point in the chain exists, and the total number of carbons in the chain is indicated by a range of numbers. In exemplary embodiments, “alkyl” refers to an alkyl chain as defined above containing 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 carbons (i.e., C₆-C₁₆ alkyl).

The term “alkenyl” as used herein refers to a carbon chain containing one or more carbon-carbon double bonds.

The term “aryl” as used herein refers to a cyclic hydrocarbon, where the ring is characterized by delocalized % electrons (aromaticity) shared among the ring members, and wherein the number of ring atoms is indicated by a range of numbers. In exemplary embodiments, “aryl” refers to a cyclic hydrocarbon as described above containing 6, 7, 8, 9, or 10 ring atoms (i.e., C₆-C₁₀ aryl). Examples of an aryl group include, but are not limited to, benzene, naphthalene, tetralin, indene, and indane.

The term “alkoxy” as used herein refers to —O-(alkyl), wherein “alkyl” is as defined above.

The term “substituted” in connection with a moiety as used herein refers to a further substituent which is attached to the moiety at any acceptable location on the moiety. Unless otherwise indicated, moieties can bond through a carbon, nitrogen, oxygen, sulfur, or any other acceptable atom.

The term “amino acid” refers to both natural (genetically encoded) and non-natural (non-genetically encoded) amino acids, and moieties thereof. Of the twenty natural amino acids, 19 have the general structure:

where R is the amino acid sidechain.

The 20^(th) amino acid, proline, is also within the scope of the present invention, and has the following structure:

Of the twenty natural amino acids, all but glycine is chiral, and both the D- and L-amino acid isomers, as well as mixtures thereof, are amenable for use with the prostacyclin compounds described herein. It is also noted that an amino acid moiety is encompassed by the term “amino acid.” For example, the amino acid moieties

are encompassed by the term “amino acid.”

Examples of non-natural amino acids amenable for use with the present invention include β-alanine (β-Ala); 2,3-diaminopropionic acid (Dpr); nipecotic acid (Nip); pipecolic acid (Pip); ornithine (Om); citrulline (Cit); t-butylalanine (t-BuA); 2-tbutylglycine (t-BuG); N-methylisoleucine (Melle); phenylglycine (PhG); eyelohexylalanine (ChA); norleucine (Nle); naphthylalanine (Nal); 4-chlorophenylalanine (Phe(4-Cl)); 2-fluorophenylalanine (Phe(2F)); 3-fluorophen yl.alani.ne (Phe(3-F)); 4fluorophenyl alanine (Phe( 4-F)); penicillamine (Pen); 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic); β-2-thienylalanine (Thi); methionine sulfoxide (MSO); homoarginine (hArg); N-acetyllysine (AcLys); 2,4-diaminobutyric acid (Dbu); 2,3-diaminobutyric acid (Dab); p-aminophenylalanine (Phe (pNH₂)): N-methyl valine (MeVal); homocysteine (hCys), homophenylalanine (hPhe); homoserine (hSer); hydroxyproline (Hyp); homoproline (hPro); and the corresponding D-enantiomer of each of the foregoing. Other non-genetically encoded amino acid residues include 3-aminopropionic acid; 4-aminobutyric acid; isonipecotic acid (Inp); aza-pipecolic acid (azPip); aza-proline (azPro); a-aminoisobutyric acid (Aib); ε-aminohexanoic acid (Aha); δ-ami.novaleric acid (Ava); N-methyl glycine (MeGly).

A “peptide” is a polymer of amino acids (or moieties thereof) linked by a peptide bond. Peptides for use with the present invention, comprise from about two to about fifteen amino acids, for example, two, three, four, five, six, seven, eight, nine or ten amino acids (or moieties thereof).

The term “salt” or “salts” as used herein encompasses pharmaceutically acceptable salts commonly used to form alkali metal salts of free acids and to form addition salts of free bases. The nature of the salt is not critical, provided that it is pharmaceutically acceptable. Suitable pharmaceutically acceptable acid addition salts may be prepared from an inorganic acid or from an organic acid. Exemplary pharmaceutical salts are disclosed in Stahl, P. H., Wermuth, C. G., Eds. Handbook of Pharmaceutical Salts: Properties, Selection and Use; Verlag Helvetica Chi.rn.ica Acta/Wiley-VCH: Zurich, 2002, the contents of which are hereby incorporated by reference in their entirety. Specific non-limiting examples of inorganic acids are hydrochloric, hydrobromie, hydroiodic, nitric, carbonic, sulfuric and phosphoric acid. Appropriate organic acids include, without limitation, aliphatic, cycloaliphatic, aromatic, arylaliphatic, and heterocyclyl containing carboxylic acids and sulfonic acids, for example formic, acetic, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, mesylic, stearic, salicylic, cycloxybenzoic, phenylacetic, mandelic, embonic (pamoic), methanesulfonic, ethanesulfonic, benzenesulfonic, pantothenic, toiuenesuifonic, 2-hydroxyethanesulfonic, sulfanilic, cyclohexylaminosulfonic, algenic, 3-hydroxybutyric, galactaric or galacturonic acid. Suitable pharmaceutically acceptable salts of free acid-containing compounds disclosed herein include, without limitation, metallic salts and organic salts. Exemplary metallic salts include, but are not limited to, appropriate alkali metal (group la) salts, alkaline earth metal (group IIa) salts, and other physiological acceptable metals. Such salts can be made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc. Exemplary organic salts can be made from primary amines, secondary amines, tertiary amines and quaternary ammonium salts, for example, tromethamine, diethylamine, tetra-N-methylammonium, N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, meglumine (N-methylglucamine) and procaine.

In one aspect, the present invention provides a prostacyclin compound, for example, a treprostinil derivative, or a composition comprising the same, that is effective when employed in a once-daily, twice-daily or three-times daily dosing regimen, for example, for the treatment of pulmonary arterial hypertension or portopulmonary hypertension in a patient in need thereof. The prostacyclin compound provided herein, in one embodiment, can be administered less frequently than treprostinil, with equal or greater efficacy. Moreover, in one embodiment, the side effect, profile of the compounds provided herein is less deleterious than the side effect profile resulting from treprostinil administration. These advantages, in one embodiment, allow for greater patient compliance. Treatment, in one embodiment, occurs through pulmonary administration of one of the compounds provided herein, for example via a nebulizer, dry powder inhaler, or a metered dose inhaler. In some embodiments, a composition comprising one of the compounds provided herein is administered via a nebulizer to a patient in need of PH treatment. In some embodiments a compound described herein is suspended in a propellant and delivered to a patient via a metered dose inhaler.

In one aspect of the invention described herein, a prostacyclin compound of Formula (I), or a pharmaceutically acceptable salt thereof, is provided:

wherein R₁ is NH, O or S;

R₂ is H, a linear C₅-C₁₈ alkyl, branched C₅-C₁₈ alkyl, linear C₂-C₁₈ alkenyl, branched C₃-C₁₈ alkenyl, aryl, aryl-C₁-C₁₈ alkyl; an amino acid or a peptide;

R₃ is H, OH, optionally substituted linear or branched C₁-C₁₅ alkyoxy, O-optionally substituted linear or branched C₂-C₁₅ alkenyl, O—(C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or O—(C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl;

R₄ is an optionally substituted linear or branched C₁-C₁₅ alkyl, or an optionally substituted linear or branched C₂-C₁₅ alkenyl; and

n is an integer from 0 to 5, with the proviso that the prostacyclin compound of Formula (I) is not treprostinil.

In a further embodiment, a prostacyclin compound of Formula (I) is provided, wherein R₃ is OH and n is 0 or 1. In even a further embodiment, R₄ is an optionally substituted linear or branched C₁-C₁₅ alkyl. In even a further embodiment, R₁ is NH or O.

In one embodiment, a prostacyclin compound of Formula (I) is provided, wherein R₁ is NH, O or S; R₂ is a linear C₅-C₁₈ alkyl, branched C₅-C₁₈ alkyl, linear C₂-C₃₈ alkenyl, branched C₃-C₁₈ alkenyl; R₃ is H, OH or O-alkyl; R₄ is an optionally substituted linear or branched C₁-C₁₅ alkyl, or an optionally substituted linear or branched C₂-C₁₅ alkenyl; and n is an integer from 0 to 5. In even a further embodiment, R₃ is NH or O and R₂ is a linear C₅-C₁₈ alkyl or a branched C₅-C₁₈ alkyl.

In one embodiment, R₂ is aryl or aryl-C₁-C₁₈ alkyl; R₃ is OH and n is 0 or 1. In even a further embodiment, R₄ is an optionally substituted linear or branched C₁-C₁₅ alkyl.

In one embodiment, the present invention provides a prostacyclin compound of Formula (I), wherein the compound is a compound of one of Formulae (Ia), (Ib), (Ic) or (Id), or a pharmaceutically acceptable salt thereof:

wherein, R₂ is H, a linear or branched C₅-C₁₈ alkyl, linear C₂-C₁₈ alkenyl, or a branched C₃-C₁₈ alkenyl;

R₃ is H, OH, optionally substituted linear or branched C₁-C₁₅ alkyoxy, O-optionally substituted linear or branched C₂-C₁₅ alkenyl, —O(C═O)-optional.ly substituted linear or branched C₁-C₁₅ alkyl, or —O(C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl; and

R₄ is

an optionally substituted linear or branched C₁-C₁₅ alkyl, or an optionally substituted linear or branched C₂-C₁₅ alkenyl, where R₅ is H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₂-C₁₅ alkenyl, (C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or (C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl. In a further embodiment, R₄ is

with the proviso that the compound is not treprostinil, i.e., R₂ and R₅ cannot both be H.

In one embodiment of Formula (Ia), Formula (Ib), Formula (Ic) and Formula (Id), R₂ is a linear or branched C₅-C₁₈ alkyl. In even a further embodiment, R₂ is

where m1 and m2 are each independently an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl. In even a further embodiment, R₂ is

and m1 and m2 are both 4. In another embodiment, R₂ is

and m1 is 3 and m2 is 4, or m1 is 2 and m2 is 3.

When m1 and/or m2 is an integer from 2-9, the m1/m2 at the end of the carbon chain is CH₃, while the remaining m1/m2 groups are CH₂.

In one embodiment of Formula (Ia), Formula (Ib). Formula (Ic) and Formula (Id), R₂ is

In a further embodiment, R₃ is OH and R₄ is

where R₅ is H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₂-C₁₅ alkenyl, (C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or (C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl.

In one embodiment of Formulae (Ia), (Ib), (Ic) or (Id), R₂ is H, R₃ is OH and R₄ is

and R₅ is

where m1 and m2 are each independently an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl. When m1 and/or m2 is an integer from 2-9, the m1/m2 at the end of the carbon chain is CH₃, while the remaining m1/m2 groups are CH₂.

In another embodiment, a prostacyclin compound of one of Formula (Ia), (Ib), (Ic) or (Id) is provided wherein R₃ is OH, as provided in one of Formulae (Ia′), (Ib′), (Ic′) or (Id′):

wherein, R₂ is H, a linear or branched C₅-C₁₈ alkyl, or a linear or branched C₅-C₁₅ alkenyl; and R₄ is

an optionally substituted linear or branched C₁-C₁₅ alkyl, or an optionally substituted linear or branched C₂-C₁₅ alkenyl, wherein R₅ is H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₂-C₁₅ alkenyl, (C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or (C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl, with the proviso that R₂ and R₅ are not both H. In one embodiment of Formula (Ia′), Formula (Ib′), Formula (Ic′) and Formula (Id′), R₄ is

and R₂ is

or R₅ is

where m1 and m2 are each independently an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl. In even a further embodiment, R₂ is

Yet another embodiment of the invention relates to a prostacyclin compound of one of Formula (Ia″), (Ib″), (Ic″) or (Id″), or a pharmaceuticaily acceptable salt thereof:

wherein,

R₂ is H, a linear or branched C₅-C₁₈ alkyl, linear C₂-C₁₈ alkenyl, branched C₃-C₁₈ alkenyl, aryl, aryl-C₁-C₁₈ alkyl; an amino acid or a peptide; and

R₃ is H, OH, optionally substituted linear or branched C₁-C₁₅ alkyoxy, O-optionally substituted linear or branched C₂-C₁₅ alkenyl, O—(C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or O—(C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl; and

R₅ is H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₁-C₁₅ alkenyl, (C═O)-optionally substituted linear or branched C₁-C₁₅alkyl, or (C═O)-optionally substituted linear or branched C₂-C₁₅ alkenyl, with the proviso that R₂ and R₅ are not both H. In a further embodiment, R₃ is OH and R₂ is 5-nonanyl, 4-heptyl, 4-octyl, 3-octyl, 2-dimethyl-1-propyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, 3-pentyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl. In even a further embodiment, R₂ is decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl. In even a further embodiment. R₂ is a linear alkyl.

One embodiment of the present invention is directed to compounds of Formula (Ic), (Ic′) and (Ic″). In a further embodiment, R₂ is a linear C₅-C₁₈ alkyl or a branched C₅-C₁₈ alkyl. In even a further embodiment, R₂ is a linear C₆-C₁₈ alkyl or a branched C₆-C₁₈ alkyl. In yet a further embodiment, R₂ is a linear C₆-C₁₄ alkyl, e.g., a linear C₆ alkyl, C₈ alkyl, C₁₀ alkyl, C₁₂ alkyl or C₁₄ alkyl.

In one embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a linear C₅-C₁₈ alkyl; R₃ is OH and R₅ is H. In another embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a linear C₆-C₁₈ alkyl; R₃ is OH and R₅ is H. In yet embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a linear C₆-C₁₆ alkyl; R₃ is OH and R₅ is H. In even another embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a linear C₈-C₁₄ alkyl; R₃ is OH and R₅ is OH.

In one embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a linear C₅-C₁₈ alkyl; R₃ is OH and R₅ is H. In another embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a branched C₆-C₁₈ alkyl; R₃ is OH and R₅ is H. In yet embodiment, a compound of Formula (Ic″) is provided wherein R₂ is a branched C₆-C₁₆ alkyl; R₃ is OH and R₅ is H. In even another embodiment, a compound of Formula (Ic″) is provided wherein R₂is a branched C₈-C₁₄ alkyl; R₃ is OH and R₅ is H.

In even a further embodiment, a compound of Formula (Ic), (Ic′) and (Ic″) is administered to a patient in need of PH treatment via a metered dose inhaler.

In yet another embodiment of Formula (Ia″), (Ib″), (Ic″) or (Id″), R₃ is OH, R₅ is H and R₂ is

where m1 and m2 are each independently an integer selected from 1 to 9. In even a further embodiment, R₂ is

In yet another embodiment of Formula (Ia″), (Ib″), (Ic″) or (Id″), R₂ is H, R₃ is OH, and R₅ is

where m1 and m2 are each independently an integer selected from 1 to 9. In even a further embodiment, R₂ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided where R₂ is a linear or branched C₅-C₁₈ alkyl. In a further embodiment, R₂ is 5-nonanyl, 4-heptanyl, 4-octanyl, 3-octanyl, 2-dimethyl-1-propanyl, 3,3-dimethyl-1-butanyl, 2-ethyl-1-butanyl, 3-pentanyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl.

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″) or (Id″) is provided where R₂ is a linear or branched C₅-C₁₈ alkyl. In even a farther embodiment, R₂ is a linear C₅-C₁₈ alkyl. In another embodiment, R₂ is

where m1 and m2 are each independently an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl. In even a further embodiment, R₂ is

In another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided wherein R₂ is a branched C₅-C₁₈ alkyl. In a further embodiment, R₂ is 5-nonanyl, 4-heptyl, 4-octyl, 3-octyl, 2-dimethyl-1-propyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, 3-pentyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl.

In one embodiment of the invention, the prostacyclin compound of the invention has the following structure:

wherein R₃ is NH, O or S.

For example, R₁ is O or N, and one of the following compounds (5-nonanyl treprostinil (alkyl ester, 5C₉-TR) or 5-nonanyl treprostlnil (amide linked; 5C9-TR-A), is provided:

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided wherein R₂ is

where m1 and m1 are each

independently each an integer selected from 1 to 9 and each occurrence of R′ is independently H, a linear or branched C₁-C₈ alkyl, or a linear or branched C₁-C₈ alkenyl.

When m1 and/or m1 is an integer from 2-9, the m1/m2 at the end of the carbon chain is CH₃, while the remaining m1/m2 groups are CH₂.

In even another embodiment, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″) or (Id″) is provided and R₂ is

The compounds provided herein can include a symmetrical branched alkyl or an asymmetrical branched alkyl as the R₂ moiety. For example, where R₂ is

m1 and m2 can be the same integer and R₂ is therefore a symmetrical branched alkyl. R₂ is an assymetrical branched alkyl when m1 and m2 are different.

In another embodiment, a compound of Formula (I). (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″) or (Id″) is provided, R₂ is

m1 is 2 and m2 is 3, m1 and m2 are each independently 4, or m1 and m2 are each independently 3.

In another embodiment, the prostacyclin compound comprises an asymmetrical branched alkyl at the R₂ position, such as, for example, 3-hexanyl (3C₆), 2-heptanyl (2C₇), 3-heptanyl (3C₇), 2-octanyl (2C₈), 3-octanyl (3C₈), or 4-octanyl (4C₈).

In another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided wherein R₂ is a branched alkyl selected from 2,2-diethyl-1-pentyl, 3-pentyl, 4-octyl, 5-nonanyl, 2-ethyl-1-butyl, 2-propyl-1-pentyl, 12-butyl-1-octyl, 2-dimethyl-1-propyl, and 3,3-dimethyl-1-butyl.

In another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′) or (Id′) is provided, wherein, R₂ is a linear or branched C₅-C₁₈ alkenyl. For example, in one embodiment, R₂ is a linear C₅-C₁₈ alkenyl selected from pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl or octadecenyl. In a further embodiment, R₃ is OH. In another embodiment, R₂ is a branched C₅-C₁₈ alkenyl selected from pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl or octadecenyl. In a further embodiment, R₃ is OH.

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided and R₄ is

In a further embodiment, R₄ is

In one embodiment, a prostacyclin compound of Formula (1), (Ia), (Ib), (Ic) or (Id) is provided and R₂ a linear C₅-C₁₈ alkyl, R₃ is OH and R₄ is

In a further embodiment, R₂ is 5-nonanyl, 4-heptyl, 4-octanyl, 3-octanyl, 2-dimethyl-1-propyl, 3,3-dimethyl-1-butyl, 2-ethyH-butyl, 3-pentyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl.

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided and R₂ hexyl, dodecyl, tetradecyl, hexadecyl, 5-nonanyl, 4-heptanyl, 4-octanyl, 3-octanyl, 2-dimethyl-1-propyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, 3-pentyl, R₃ is OH and R₄ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided and R₂ hexyl, R₃ is OH and R₄ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id) is provided and R₂ hexyl, R₃ is OH and R₄ is

In another embodiment, a prostacyclin compound of Formula (Ia″), (Ib″), (Ic″) or (Id″) is provided and R₂ hexyl, R₃ is OH R₄ is H. In a further embodiment, the compound is a compound of Formula (Ic″). In yet another embodiment, a prostacyclin compound of Formula (Ia″), (Ib″), (Ic″) or (Id″) is provided and R₂ dodecyl, tetradecyl, pentadecyl or hexadecyl, R₃ is OH R₄ is H. In a further embodiment, the compound is a compound of Formula (Ia″). In even a further embodiment, the compound is present in a lipid nanoparticle formulation as described in more detail below.

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ heptyl, R₃ is OH and R₄ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ octyl, R₃ is OH and R₄ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ nonyl, R₃ is OH and R₄ is

In another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ decyl, R₃ is OH and R₄ is

In yet another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ undecyl, R₃ is OH and R₄ is

In even another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ dodecyl, R₃ is OH and R₄ is

In one embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ tridecyl, R₃ is OH and R₄ is

In another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), or (Id), or pharmaceutically acceptable salt, is provided, and R₂ tetradecyl, R₃ is OH and R₄ is

In even another embodiment, a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or pharmaceutically acceptable salt, is provided, and R₂ pentadecyl, R₃ is OH and R₄ is

Another embodiment of the invention concerns a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), aor pharmaceutically acceptable salt, wherein R₂ hexadecyl, R₃ is OH and R₄ is

Yet another embodiment of the invention concerns a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), a or pharmaceutically acceptable salt, wherein R₂ heptadecyl, R₃ is OH and R₄ is

Yet another embodiment of the invention concerns a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or a pharmaceutically acceptable salt, wherein R₂ octadecyl, R₃ is OH and R₄ is

In one embodiment, a compound of Formula (I), (Ia), (Ib), (Ic) or (Id), or a pharmaceutically acceptable salt, is provided, wherein one or more hydrogen atoms is substituted with a deuterium. Accordingly, in one embodiment, the present invention relates to an isotopologue of Formula (I), (Ia), (Ib), (Ic) or (Id), substituted with one or more deuterium atoms. The isotopologue of Formula (I), (Ia), (Ib), (Ic) or (Id) may be used to accurately determine the concentration of compounds of Formula (I), (Ia), (Ib), (Ic ) or (Id) in biological fluids and to determine metabolic patterns of compounds of Formula (I), (Ia), (Ib), (Ic) or (Id) and its isotopologues. The invention further provides compositions comprising these deuterated isotopologues and methods of treating diseases and conditions, as set forth herein.

In another aspect of the invention, a prostacyclin compound of Formula (II), or a pharmaceutically acceptable salt thereof, is provided:

wherein R₁ is NH, O or S;

R₂ is a linear or branched C₅-C₁₈ alkyl, a linear C₂-C₁₈ alkenyl or a branched C₃-C₁₈ alkenyl, aryl, aryl-C₁-C₁₈ alkyl, an amino acid or a peptide; and n is an integer from 0 to 5.

In one embodiment, a prostacyclin compound of Formula (II), or a pharmaceutically acceptable salt thereof, is provided, wherein R₁ is NH, O or S; R₂ is a linear or branched C₅-C₁₈ alkyl, a linear C₂-C₁₈ alkenyl or a branched C₃-C₁₈ alkenyl; and n is an integer from 0 to 5. In a further embodiment, n is 1 and R₁ is NH or O.

In one embodiment, the present invention relates to the prostacyclin compound of Formula (II), wherein the compound is a compound of formula (IIa), (IIb), (IIc) or (IId), or a pharmaceutically acceptable salt thereof:

wherein R₂ is a linear or branched C₅-C₁₈ alkyl, a linear C₂-C₁₈ alkenyl or a branched C₃-C₁₈ alkenyl, aryl, aryl-C₁-C₁₈ alkyl, an amino acid or a peptide. In a further embodiment, a compound of formula (Ila), (IIb), (IIc) or (IId) is provided wherein R₂ is a linear or branched C₅-C₁₈ alkyl, a linear C₂-C₁₈ alkenyl or a branched C₃-C₁₈ alkenyl. In one embodiment, a compound of Formula (II), (IIa), (IIb), (IIc) or (IId) is provided, wherein one or more hydrogen atoms is substituted with a deuterium. Accordingly, in one embodiment, the present invention relates to an isotopologue of Formula (II), (IIa), (IIb), (IIc) or (IId), substituted with one or more deuterium atoms. The isotopologue of Formula (II), (IIa), (IIb), (IIc) or (IId) may be used to accurately determine the concentration of compounds of Formula (II), (IIa), (IIb), (IIc) or (IId) in biological fluids and to determine metabolic patterns of compounds of Formula (II), (IIa), (IIb), (IIc) or (IId) and its isotopologues. The invention further provides compositions comprising these deuterated isotopologues and methods of treating diseases and conditions, as set forth herein.

In one embodiment, the prostacyclin derivative is a compound of Formula (IIc). In a further embodiment, R₂ is a linear C₅-C₁₈ alkyl or a branched C₅-C₁₈ alkyl. For example, in one embodiment, R₂ is a linear C₆-C₁₈ alkyl. In another embodiment of Formula (IIc), R₂ is a linear C₆-C₁₀ alkyl. In even a further embodiment of Formula (IIc), R₂ is a hexyl, heptyl or octyl.

Compounds of Formula (IIa) and Formula (IId) are provided in tables A and B below.

TABLE A Compounds of Formula (IIa) R₂ ₌ linear C₅-C₁₈ alkyl R₂ ₌ branched C₅-C₁₈ alkyl R₂ ₌ linear C₈ alkyl R₂ ₌ branched C₆ alkyl R₂ ₌ linear C₆-C₁₈ alkyl R₂ ₌ branched C₆-C₁₈ alkyl R₂ ₌ linear C₉ alkyl R₂ ₌ branched C₇ alkyl R₂ ₌ linear C₇-C₁₈ alkyl R₂ ₌ branched C₇-C₁₈ alkyl R₂ ₌ linear C₁₀ alkyl R₂ ₌ branched C₈ alkyl R₂ ₌ linear C₈-C₁₈ alkyl R₂ ₌ branched C₈-C₁₈ alkyl R₂ ₌ linear C₁₁ alkyl R₂ ₌ branched C₉ alkyl R₂ ₌ linear C₉-C₁₈ alkyl R₂ ₌ branched C₉-C₁₈ alkyl R₂ ₌ linear C₁₂ alkyl R₂ ₌ branched C₁₀ alkyl R₂ ₌ linear C₁₀-C₁₈ alkyl R₂ ₌ branched C₁₀-C₁₈ alkyl R₂ ₌ linear C₁₃ alkyl R₂ ₌ branched C₁₁ alkyl R₂ ₌ linear C₁₁-C₁₈ alkyl R₂ ₌ branched C₁₁-C₁₈ alkyl R₂ ₌ linear C₁₄ alkyl R₂ ₌ branched C₁₂ alkyl R₂ ₌ linear C₁₂-C₁₈ alkyl R₂ ₌ branched C₁₂-C₁₈ alkyl R₂ ₌ linear C₁₅ alkyl R₂ ₌ branched C₁₃ alkyl

TABLE B Compounds of Formula (IIc) R₂ ₌ linear C₅-C₁₈ alkyl R₂ ₌ branched C₅-C₁₈ alkyl R₂ ₌ linear C₆ alkyl R₂ ₌ branched C₆ alkyl R₂ ₌ linear C₆-C₁₈ alkyl R₂ ₌ branched C₆-C₁₈ alkyl R₂ ₌ linear C₇ alkyl R₂ ₌ branched C₇ alkyl R₂ ₌ linear C₇-C₁₈ alkyl R₂ ₌ branched C₇-C₁₈ alkyl R₂ ₌ linear C₈ alkyl R₂ ₌ branched C₈ alkyl R₂ ₌ linear C₈-C₁₈ alkyl R₂ ₌ branched C₈-C₁₈ alkyl R₂ ₌ linear C₉ alkyl R₂ ₌ branched C₉ alkyl R₂ ₌ linear C₉-C₁₈ alkyl R₂ ₌ branched C₉-C₁₈ alkyl R₂ ₌ linear C₁₀ alkyl R₂ ₌ branched C₁₀ alkyl R₂ ₌ linear C₁₀-C₁₈ alkyl R₂ ₌ branched C₁₀-C₁₈ alkyl R₂ ₌ linear C₁₁ alkyl R₂ ₌ branched C₁₁ alkyl R₂ ₌ linear C₅-C₁₂ alkyl R₂ ₌ branched C₅-C₁₂ alkyl R₂ ₌ linear C₁₂ alkyl R₂ ₌ branched C₁₂ alkyl R₂ ₌ linear C₆-C₁₀ alkyl R₂ ₌ branched C₆-C₁₀ alkyl R₂ ₌ linear C₁₃ alkyl R₂ ₌ branched C₁₃ alkyl

Yet another embodiment of the invention relates to a prostacyclin compound of Formula (III), or a pharmaceutically acceptable salt thereof:

wherein R₁ and R₂ are defined as provided for Formula (I) and (II), and

R₅ and R₆ are independently selected from H, optionally substituted linear or branched C₁-C₁₅ alkyl, optionally substituted linear or branched C₂-C₁₅ alkenyl, (C═O)-optionally substituted linear or branched C₁-C₁₅ alkyl, or (C═O)-optionalIy substituted linear or branched C₂-C₁₅ alkenyl, with the proviso that the prostacyclin compound of Formula (III) is not treprostinil.

In one embodiment, the branched chain prostacyclin compounds provided herein exhibit both higher solubility and slower enzymatic conversion to treprostinil relative to a linear chain derivatized prostacyclin compound. In one embodiment, an asymmetrical branched chain prostacyclin compound is provided, wherein the asymmetrical branched chain prostacyclin compound is more stable than a corresponding symmetrical branched chain prostacyclin compound.

In one embodiment, the present invention provides prostacyclin compounds that contain a chiral moiety at one or more of the R₂, R₅ and/or R₆ positions. For example, the moiety at position R₂, in one embodiment, is a chiral moiety and comprises either the R isomer, the S isomer, or a mixture thereof. An optical isomer at position R₂, R₅ and/or R₆ can also be classified with the D/L nomenclature. For example, where R₂ is an amino acid or an amino acid moiety, the amino acid or amino acid moiety can be the D-isomer, L-isomer, or a mixture thereof.

In one embodiment, one or more of the R₂, R₅ and/or R₆ moieties is the R isomer or S isomer. In another embodiment, one or more of the R₂, R₅ and/or R₆ moieties provided herein comprise a mixture of R and S moieties. The “R isomer” or “S isomer” as used herein refers to an enantiomerically pure isomer. An “enantiomerically pure isomer” has at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% pure R- or S-isomer or when using the D/L nomenclature, D- or L-isomer. A racemic compound is a compound having a mixture in equal amounts of both enantiomers.

In another aspect of the invention, the prostacyclin compound described herein is provided in a composition, for example, for delivery to a patient for the treatment of pulmonary hypertension (PH). Compositions can include the compound, a pharmaceutically acceptable salt of the compound, or a combination thereof. In one embodiment, the PH is pulmonary arterial hypertension (PAH), Prostacyclin compositions (so called “lipid nanoparticle compositions”) and formulations comprising a prostacyclin, a cationic compound, and a surfactant have been described in PCT publication no. WO 2014/085813, the disclosure of which is hereby incorporated by reference in its entirety for all purposes. The compositions described in WO 2014/085813 are amenable for use with the prostacyclin derivative compounds provided herein.

In one embodiment, the composition comprises one of the prostacyclin compounds described herein, i.e., a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), and an amphiphilic agent. When formulated together, in one embodiment, the prostacyclin compound and amphiphilic agent form micro- or nanoparticles. In one embodiment, the amphiphilic agent is a PEGylated lipid, a surfactant or a block copolymer. In another embodiment, the prostacyclin composition provided herein comprises two or more of the prostacyclin compounds described herein (e.g., a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), including deuterated compounds) and an amphiphilic agent (e.g., PEGylated lipid, a lipid, a surfactant or a block copolymer). In one embodiment, the prostacyclin composition comprising the prostacyclin compound component and amphiphilic agent, when formulated together, comprise a plurality of nanoparticles. In a further embodiment, the mean diameter of the plurality of nanoparticles is from about 20 nm to about 700 nm, for example about 50 nm to about 500 nm, about 100 nm to about 600 nm or about 100 nm to about 500 nm. When the amphiphilic agent comprises a lipid, e.g., a PEGylated lipid such as Cholesterol-PEG or distearoylphosphatidylethanolamine-PEG (DSPE-PEG), the composition is described as comprising lipid nanoparticles.

In a further embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), and a PEGylated lipid as the amphilphilic agent. In a further embodiment, the PEGylated lipid comprises PEG400-PEG5000. For example, in one embodiment, the PEGylated lipid comprises PEG400, PEG500, PEG 1000, PEG2000, PEG3000, PEG4000, or PEG5000. In a further embodiment the lipid component of the PEGylated lipid comprises cholesterol, dimyristoyl phosphatidylethanolamine (DMPE), dipaimitoyl phosphoethanolamine (DPPE), distearoylphosphatidylethanolamine (DSPE), dimyristoylglycerol glycerol (DMG), diphosphatidylglycerol (DPG) or disteraroylglycerol (DSG). In even a further embodiment, the PEGylated lipid is cholesterol-PEG2000 or DSPE-PEG2000.

Depending on its molecular weight (MW), PEG is also referred to in the art as polyethylene oxide (PEO) or polyoxyethylene (POE), The PEGylated lipid can include a branched or unbranched PEG molecule, and is not limited by a particular PEG MW.

For example, the PEGylated lipid, in one embodiment, comprises a PEG molecule having a molecular weight of 300 g/mol, 400 g/mol, 500 g/mol, 1000 g/mol, 1500g/mol, 2000 g/mol, 2500 g/mol, 3000 g/mol, 3500 g/mol, 4000 g/mol, 4500 g/mol, 5000 g/mol or 10,000 g/mol. In one embodiment, the PEG has a MW of 1000 g/mol or 2000 g/mol.

The lipid component of the PEGylated lipid, can have a net-charge (e.g., cationic or anionic), or can be net-neutral. The lipids used in the PEGylated lipid component of the present invention can be synthetic, semi-synthetic or naturally-occurring lipid, including a phospholipid, a sphingolipid, a glycolipid, a ceramide, a tocopherol, a sterol, a fatty acid, or a glycoprotein such as albumin. In one embodiment, the lipid is a sterol. In a further embodiment, the sterol is cholesterol. In another embodiment, the lipid is a phospholipid. Phospholipids include, but are not limited to phosphatidylcholine (PC), phosphatidylglycerol (PG), phosphatidylinositol (PI), phosphatidylserine (PS), phosphatidylethanoiarnine (PE), and phosphatidic acid (PA). In one embodiment, the phospholipid is an egg phospholipid, a soya phospholipid or a hydrogenated egg and soya phospholipid. In one embodiment, the PEGylated lipid comprises a phospholipid. In a further embodiment, the phospholipid comprises ester linkages of fatty acids in the 2 and 3 of glycerol positions containing chains of 12 to 26 carbon atoms and different head groups in the 1 position of glycerol that include choline, glycerol, inositol, serine, ethanolamine, as well as the corresponding phosphatidic acids. The chains on these fatty acids can be saturated or unsaturated, and the phospholipid can be made up of fatty acids of different chain lengths and different degrees of unsaturation. In particular, in one embodiment, the PEGylated lipid of the prostacyclin composition provided herein comprises distearoylphosphoethanolamine (DSPE), dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine (DOPC) dimyristoyl phosphatidylethanoiarnine (DMPE), dipalmitoylphosphoethanolamine (DPPE), distearoylphosphatidylethanolamine (DSPE), dimyristoylglycerol (DMG), diphosphatidylglycerol (DPG) or disteraroylglycerol (DSG).

Other examples of lipids for use in the compositions comprising PEGylated lipids disclosed herein include dimyristoylphosphatidylcholine (DMPC), dimyristoylphosphatidylglycerol (DMPG), dipalmitoylphosphatidylglycerol (DPPG), distearoylphosphatidylcholine (DSPC), distearoylphosphatidylglycerol (DSPG) dioleylphosphatidylethanolamine (DOPE), and mixed phospholipids such as palmitoylstearoylphosphatidylcholine (PSPC) and palmitoylstearoylphosphatidylglycerol (PSPG), triacylglycerol, diacylglycerol, eeramide, sphingosine, sphingomyelin and single aeylated phospholipids such as mono-oleoyl-phosphatid.ylethanolam.ine (MOPE). In another embodiment lipid portion of the PEGylated lipid comprises an ammonium salt of a fatty acid, a phospholipid, a glyceride, a phospholipid and glyceri.de, a sterol (e.g., cholesterol), phosphatidyl glycerol (PG), phosphatide acid (PA), a phosphotidyfcholine (PC), a phosphatidylinositol (PI), a phosphatidylserine (PS), or a combination thereof. The fatty acid, in one embodiment, comprises fatty acids of carbon chain lengths of 12 to 26 carbon atoms that are either saturated or unsaturated. Some specific examples include: myristylamine, palmitylamine, laurylamine and stearylamine, dilauroyl ethylphosphocholine (DLEP), dimyristoyl ethylphosphocholine (DMEP), dipalmitoyl ethylphosphocholine (DPEP) and distearoyl ethylphosphocholine (DSEP), N-(2,3-di-(9(Z)-octadecenyloxy)-prop-1-yl-N,N,N-trimethylammonium chloride (DOTMA) and l,2-bis(oleoyloxy)-3-(trimethylammonio)propane (DOTAP). Examples of sterols for use in the compositions provided herein include cholesterol and ergosterol. Examples of PGs, PAs, Pis, PCs and PSs for use in the compositions provided herein include DMPG, DPPG, DSPG, DMPA, DPPA, DSPA, DMPI, DP PI, DSPI, DMPS, DPPS and DSPS, DSPC, DPPG, DMPC, DOPC, egg PC and soya PC.

In one embodiment, the PEGylated lipid is cholesterol-PEG2000, DSPE-PEG1000 or DSG-PEG2000.

In another embodiment, the prostacyclin composition provided herein comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), and a hydrophobic additive. In a further embodiment, the composition comprises an amphiphilic agent, e.g., a PEGylated lipid, as described above.

In yet another embodiment, two or more of the prostacyclin compounds described herein (e.g., a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III)) an amphiphilic agent (e.g., PEGylated lipid, a lipid, a surfactant or a block copolymer) and a hydrophobic additive are provided in a composition.

In one embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III) and a PEGylated lipid. In another embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III) and a surfactant. In yet another embodiment, the prostacyclin composition comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), a hydrophobic additive and an amphiphilic agent. In a further embodiment, the amphiphilic agent is a surfactant, a PEGylated lipid or a block copolymer. In even a further embodiment, the amphiphilic agent is a PEGylated lipid.

In one embodiment, the prostacyclin compound is present in the composition at 5 mol %-99 mol %. In a further embodiment, the prostacyclin compound is present in the composition at 40 mol %-95 mol %. In a further embodiment, the prostacyclin compound is present in the composition at 40 mol %-60 mol %. In one embodiment, the prostacyclin compound is present in the composition at about 40 mol % or about 45 mol %.

The amphiphilic agent, e.g., a PEGylated lipid, when present in the composition, in one embodiment, is present at 10 mol %-30 mol %, for example, 10 mol %-20 mol % or 15 mol %-25 mol %. In even a further embodiment, the PEGylated lipid is present in the composition at about 10 mol % or 20 mol %.

The hydrophobic additive, when present in the composition, in one embodiment, is present in the composition at 25 mol %-50 mol %, for example, 30 mol %-50 mol %, 35 mol %-45 mol %. In even a further embodiment, the hydrophobic additive is present in the composition at about 40 mol % or about 45 mol %.

The prostacyclin composition, in one embodiment, comprises a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a pharmaceutically acceptable salt thereof, as described herein, an amphophilic agent and a hydrophobic additive. In one embodiment, the hydrophobic additive (e.g., an additive that is at least partially hydrophobic) is a hydrocarbon, a terpene compound or a hydrophobic lipid (e.g., tocopherol, tocopherol acetate, sterol, sterol ester, alkyl ester, vitamin A acetate, a triglyceride, a phospholipid). In one embodiment, the composition comprises a prostacyclin compound, for example, a compound of Formula (I) or (II), an amphiphilic agent, and a hydrocarbon. The hydrocarbon can be aromatic, an alkane, alkene, cycloalkane or an alkyne. In one embodiment, the hydrocarbon is an alkane (i.e., a saturated hydrocarbon). In another embodiment, the hydrocarbon is a C₁₅-C₅₀ hydrocarbon.

In a further embodiment, the hydrocarbon is a C₁₅, C₂₀, C₂₅, C₃₀, C₃₅, C₄₀, C₄₅ or C₅₀ hydrocarbon. In yet another embodiment, the hydrophobic additive is a C₁₅-C₂₅ hydrocarbon, C₁₅-C₃₅ hydrocarbon, C₁₅-C₄₅ hydrocarbon, C₁₅-C₂₀ hydrocarbon, C₂₀-C₂₅ hydrocarbon, C₂₅-C₃₀ hydrocarbon, C₃₀-C₃₅ hydrocarbon, C₃₅-C₄₀ hydrocarbon, C₄₀-C₄₅ hydrocarbon or a C₄₅-C₅₀ hydrocarbon.

In one embodiment, a composition comprising a prostacyclin compound, an amphiphilic agent and a terpene compound (e.g., the hydrophobic additive) is provided. The composition, in a further embodiment, comprises a PEGylated lipid as the amphiphilic agent. However, as noted above, block copolymers as well as surfactants can be used as the amphiphilic component of the composition. The terpene compound (hydrophobic additive), in one embodiment, is a hydrocarbon (e.g., isoprene, squalaneor squalene). In another embodiment, the terpene compound is a hemiterpene (C₅H₈), monoterpene (C₁₀H₁₆), sesquiterpene (C₁₅H₂₄), diterpene (C₂₀H₃₂) (e.g., cafestol, kahweol, cembrene, taxadiene), sesterterpene (C₂₅H₄₀), triterpene (C₃₀H₄₈), sesquaterpene (C₃₅H₅₆), tetraterpene (C₄₀H₆₄), polyterpene (e.g., a polylsoprene with trans double bonds) or a norisoprenoid (e.g., 3-oxo-α-ionol, 7,8-di.hydroionone derivatives). The terpene compound, in another embodiment, is selected from one of the compounds provided in Table 1, below. In one embodiment, the hydrophobic additive is squalane.

TABLE 1 Terpene hydrophobic additives amenable for use in the compositions of the present invention. Name Formula Isoprene

Limonene

humulene

farnasene

squalene

squalane

As provided above, the composition provided herein, in one embodiment, comprises a prostacyclin compound and one or more PEGylated lipids. In a further embodiment, the composition comprises a hydrophobic additive, as described above. In one embodiment, the composition provided herein comprises a prostacyclin compound of one of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), a hydrophobic additive and a PEGylated lipid. In a further embodiment, the hydrophobic additive comprises a hydrocarbon e.g. a terpene compound.

In one embodiment, the treprostinil derivative composition provided herein includes the components provided in Table C, below.

TABLE C Representative Treprostinil Compositions. Composition Hydrophobic Amphiphilic Additional # Treprostinil compound additive agent lipid 1 Formula (II) where R₁ is O, Terpene PEGylated lipid n/a R₂ is linear C₆-C₁₆ 2 Formula (II) where R₁ is O, Terpene PEGylated lipid DOPC R₂ is linear C₆-C₁₆ 3 Formula (II) where R₁ is O, Squalane Chol-PEG2k n/a R₂ is linear C₆-C₁₆ 4 Formula (II) where R₁ is O, Squalane DSPE-PEG2k n/a R₂ is linear C₆-C₁₆ 5 Formula (II) where R₁ is O, Terpene PEGylated lipid n/a R₂ is linear C₁₀-C₁₆ 6 Formula (II) where R₁ is O, Terpene PEGylated lipid DOPC R₂ is linear C₁₀-C₁₆ 7 Formula (II) where R₁ is O, Squalane Chol-PEG2k n/a R₂ is linear C₁₀-C₁₆ 8 Formula (II) where R₁ is O, Squalane DSPE-PEG2k n/a R₂ is linear C₁₀-C₁₆ 9 Formula (II) where R₁ is O, Terpene PEGylated lipid n/a R₂ is linear C₁₂-C₁₆ 10 Formula (II) where R₁ is O, Terpene PEGylated lipid DOPC R₂ is linear C₁₂-C₁₆ 11 Formula (II) where R₁ is O, Squalane Chol-PEG2k n/a R₂ is linear C₁₂-C₁₆ 12 Formula (II) where R₁ is O, Squalane DSPE-PEG2k n/a R₂ is linear C₁₂-C₁₆ 13 Formula (II) where R₁ is O, Terpene PEGylated lipid n/a R₂ is branched C₆-C₁₆ 14 Formula (II) where R₁ is O, Terpene PEGylated lipid DOPC R₂ is branched C₆-C₁₆ 15 Formula (II) where R₁ is O, Squalane Chol-PEG2k n/a R₂ is branched C₆-C₁₆ 16 Formula (II) where R₁ is O, Squalane DSPE-PEG2k n/a R₂ is branched C₆-C₁₆ 17 Formula (II) where R₁ is N, Terpene PEGylated lipid n/a R₂ is linear C₆-C₁₆ 18 Formula (II) where R₁ is N, Terpene PEGylated lipid DOPC R₂ is linear C₆-C₁₆ 19 Formula (II) where R₁ is N, Squalane Chol-PEG2k n/a R₂ is linear C₆-C₁₆ 20 Formula (II) where R₁ is N, Squalane DSPE-PEG2k n/a R₂ is linear C₆-C₁₆ 21 Formula (II) where R₁ is N, Terpene PEGylated lipid n/a R₂ is linear C₆-C₁₀ 22 Formula (II) where R₁ is N, Terpene PEGylated lipid DOPC R₂ is linear C₆-C₁₀ 23 Formula (II) where R₁ is N, Squalan Chol-PEG2k n/a R₂ is linear C₆-C₁₀ 24 Formula (II) where R₁ is N, Squalane DSPE-PEG2k n/a R₂ is linear C₆-C₁₀

The present invention also provides methods for treating a patient in need thereof, with one of the prostacyclin compounds or compositions described herein. It is understood that reference to a prostacyclin compound in a treatment method includes the use of a pharmaceutically acceptable salt of the compound. Similarly, administration of a prostacyclin composition comprising a prostacyclin compound includes the use of a pharmaceutically acceptable salt in the composition.

In one aspect, a method for treating pulmonary hypertension (PH) is provided. The method comprises, in one embodiment, administration of a compound, pharmaceutically acceptable salt thereof, or composition provided herein to a patient in need thereof. Administration, in one embodiment, is pulmonary administration and can be, for example, with a metered dose inhaler (MDI), dry powder inhaled (DPI), or a nebulizer. The World Health Organization (WHO) has classified PH into five groups, WHO Group I PH includes pulmonary arterial hypertension (PAH), idiopathic pulmonary arterial hypertension (IPAH), familial pulmonary arterial hypertension (FPAH), and pulmonary arterial hypertension associated with other diseases (APAH). For example, pulmonary arterial hypertension associated with collagen vascular disease (e.g., scleroderma), congenital shunts between the systemic and pulmonary circulation, portal hypertension and/or HIV infection are included in group I PH. The methods provided herein, in one embodiment, are provided to treat a WHO Group I PH patient in need thereof, for example a PAH patient, an IPAH patient, a FPAH patient or an APAH patient, WHO Group II PH includes pulmonary hypertension associated with left heart disease, e.g., atrial or ventricular disease, or valvular disease (e.g., mitral stenosis). The methods provided herein, in one embodiment, are provided to treat a WHO Group II patient in need thereof. WHO group III pulmonary hypertension is characterized as pulmonary hypertension associated with lung diseases, e.g., chronic obstructive pulmonary disease (COPD), interstitial lung disease (ILD), and/or hypoxemia. The methods provided herein, in one embodiment, are provided to treat a WHO Group III patient in need thereof. WHO Group IV pulmonary hypertension is pulmonary hypertension due to chronic thrombotic and/or embolic disease. Group IV PH is also referred to as chronic thromboembolic pulmonary hypertension. Group IV PH patients experience blocked or narrowed blood vessels due to blood clots. The methods provided herein, in one embodiment, are provided to treat a WHO Group IV patient in need thereof. WHO categorizes Group V PH as the “miscellaneous” category, and includes PH caused by blood disorders (e.g., polycythemia vera, essential thrombocythemia), systemic disorders (e.g., sarcoidosis, vasculitis) and/or metabolic disorders (e.g., thyroid disease, glycogen storage disease). The methods provided herein, in one embodiment, are provided to treat a WHO Group V patient in need thereof.

The methods provided herein can be used to treat a WHO Group I (i.e., pulmonary arterial hypertension or PAH), Group II, Group III, Group IV or Group V PH patient. In one embodiment of the method for treating PH, a method of treating pulmonary arterial hypertension (PAH) is provided. In another embodiment, a method for treating chronic thromboembolic pulmonary hypertension patient is provided. In one embodiment, the method for treating PH (e.g., PAH) comprises administering an effective amount of one of the compounds described herein via a pulmonary (inhalation, e.g., via an MDI or nebulizer or dry powder inhaler), a subcutaneous, oral, nasal or an intravenous route of administration, to a patient in need thereof. In one embodiment, administration is via inhalation via an MDI or nebulizer. In one embodiment, where compound delivery is via a nebulizer, the compound is provided to the patient as a composition, for example, as a lipid nanoparticle composition, as described above.

In another aspect of the invention, a method for treating portopulmonary hypertension (PPH) is provided. In one embodiment, the method comprises administering an effective amount of one of the compounds described herein (or a pharmaceutically acceptable salt thereof), via a pulmonary (inhalation), a subcutaneous, oral, nasal or an intravenous route of administration, to a patient in need thereof. In one embodiment, administration is via inhalation via an MDI or nebulizer. In one embodiment, where compound delivery is via a nebulizer, the compound is provided to the patient as a composition, for example, as a lipid nanoparticle composition, as described above.

Methods for administering treprostinil and analogs thereof for treatment of pulmonary hypertension have been described in U.S. Pat. Nos, 5,153,222; 6,521,212; 7,544,713 and U.S. Patent Application Publication No. 2010/0076083, the disclosure of each are incorporated by reference in their entireties for all purposes.

The method for treating a patient for PH (e.g., PAH) or PPH comprises, in one embodiment, administering to a patient in need thereof, one of the prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), a pharmaceutically acceptable salt thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a pharmaceutically acceptable salt thereof. In one embodiment, the method for treating PH (e.g., PAH) or PPH comprises administering to a patient in need thereof, one of the prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III). Routes of administration to the patient include pulmonary (inhalation), subcutaneous, oral, nasal and intravenous. In one embodiment, administration of a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a pharmaceutically acceptable salt thereof, is via inhalation via an MDI or nebulizer. In one embodiment, where compound delivery is via a nebulizer, the compound is provided to the patient as a composition, for example, as a lipid nanoparticle composition, as described above.

In one embodiment, the method for treating PH, PAH or PPH comprises administering to a patient in need thereof, an effective amount of the prostacyclin compound or prostacyclin composition described herein. In a further embodiment, the compound, or a pharmaceutically acceptable salt of the compound, is administered to the patient via a pulmonary (inhalation), a subcutaneous, oral, nasal or an intravenous route of administration. In a further embodiment, administration is via inhalation and the prostacyclin compound or composition is administered with a nebulizer, dry powder inhaler, or MDI. In even a further embodiment the prostacyclin composition or composition comprises a prostacyclin compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof or a pharmaceutically acceptable salt of the compound ,

In one embodiment, administration of an effective amount of a prostacyclin compound or composition of the present invention for the treatment of PH, PAH or PPH via inhalation, oral, nasal, subcutaneous or intravenous administration results in a decreased number of side effects, or a reduced severity of one or more side effects (also referred to herein as “adverse events”), compared to the administration of an effective amount of treprostinil, when an effective amount of treprostinil is administered via inhalation, oral, nasal, subcutaneous, or intravenous administration. For example, in one embodiment, a PH, PAH or PPH patient experiences a reduced severity and/or frequency in cough or a reduced cough response when administered a prostacylin compound or composition of the invention via inhalation (e.g., nebulization, dry powder inhaler, or via a metered dose inhaler), compared to the severity and/or frequency of cough or cough response elicited by inhalation administration of treprostinil to the patient.

In another embodiment, oral, nasal, intravenous, subcutaneous or inhalation administration of an effective amount of the prostacyclin compound or composition of the invention, compared to oral, nasal, subcutaneous, intravenous or inhalation administration of treprostinil, results in a reduced severity of one or more of the following adverse events, or a decreased occurrence of one or more of the following adverse events: headache, throat irritation/pharyngolaryngeal pain, nausea, flushing and/or syncope.

In another embodiment, oral, nasal, intravenous, subcutaneous or inhalation administration of an effective amount of the prostacyclin compound or composition of the invention, for the treatment of PH, PAH or PPH, compared to oral, nasal, subcutaneous, intravenous or inhalation administration of treprostinil, results in a reduced severity of a systemic adverse events, or a decreased occurrence of a systemic adverse event.

Without wishing to be bound by theory, it is believed that the improved adverse event profile of the prostacylin compounds and compositions of the invention exhibited patients, as compared to treprostinil, results in improved compliance of the patients.

In one embodiment, the prostacyclin compounds and compositions of the present invention are administered on a less frequent basis, as compared to currently approved therapies for PH, PAH (e.g., Tyvaso®, Remodulin®) or PPH, while still achieving a substantially equivalent or better therapeutic response. Routes of administration to the patient include pulmonary (inhalation), subcutaneous, oral, nasal and intravenous. The therapeutic response of the patient, in one embodiment, is a reduction in the pulmonary vascular resistance index (PVRI) from pretreatment value, a reduction in mean pulmonary artery pressure from pretreatment value, an increase in the hypoxemia score from pretreatment value, a decrease in the oxygenation index from pretreatment values, improved right heart function, as compared to pretreatment or improved exercise capacity (e.g., as measured by the six-minute walk test) compared to pretreatment. The therapeutic response, in one embodiment, is an improvement of at least 10%, at least 20%, at least 30%, at least 40% or at least 50%, as compared to pretreatment values. In another embodiment, the therapeutic response is an improvement of about 10%) to about 70%, about 10% to about 60%, about 10% to about 50%, about 10% to about 40%, about 10% to about 30%, about 10% to about 20%, about 20% to about 70%, about 20% to about 60% or about 10% to about 50%, as compared to pretreatment levels.

Without wishing to be bound by theory, the l ess frequent administration of the compounds and compositions of the invention allows for improved patient compliance, as compared to the compliance of patients being administered a different PH, PAH or PPH treatment (e.g., treprostinil—Tyvaso®, Remodulin®).

In one embodiment, a composition or compound of the present invention is administered via a metered dose inhaler (MDI) to a patient in need of PH, PAH or PPH treatment. The composition or compound, in one embodiment, is delivered via a MDI by the use of a propellant, for example, a chloro-fluorocarbon (CFC) or a fluorocarbon. In one embodiment, where delivery is via an MDI, the compound is not formulated as a lipid nanoparticle composition, and instead, is suspended or dissolved directly in a propellant solution. The patient, in one embodiment, is administered the prostacyclin compound or composition of the invention once daily, twice daily or three times daily. In one embodiment, the administration is with food. In one embodiment, each administration comprises 1 to 5 doses (puffs) from an MDI, for example 1 dose (1 puff), 2 dose (2 puffs), 3 doses (3 puffs), 4 doses (4 puffs) or 5 doses (5 puffs). The MDI, in one embodiment, is small and transportable by the patient.

In another embodiment, the prostacyclin compound or prostacyclin composition is administered via a nebulizer to a patient in need of PH, PAH or PPH treatment. The administration occurs in one embodiment, once daily, twice daily, three times daily or once every other day.

In one embodiment, a composition or compound of the present invention is administered via a dry powder inhaler (DPI) to a patient in need of PH, PAH or PPH treatment. The patient, in one embodiment, is administered the prostacyclin compound or composition of the invention once daily, twice daily or three times daily. In one embodiment, the administration is with food. In one embodiment, each administration comprises 1 to 5 doses (puffs) from a DPI, for example 1 dose (1 puff), 2 dose (2 puffs), 3 doses (3 puffs), 4 doses (4 puffs) or 5 doses (5 puffs). The DPI, in one embodiment, is small and transportable by the patient.

In another embodiment, the prostacyclin compound administered to a patient

in need thereof via a pulmonary route by the PH, PAH or PAH treatment methods described herein provides a greater pulmonary elimination half-life (t_(1/2)) of the prostacyclin compound or its treprostinil metabolite, compared to the pulmonary elimination half-life (t_(1/2)) of treprostinil, when treprostinil is administered via a pulmonary route (e.g., by nebulization, dry powder inhaler, or a metered dose inhaler) to the patient in need of PH, PAH or PPH treatment.

In another embodiment, the prostacyclin compound administered to a patient in need thereof, via the PH, PAH or PPH treatment methods described herein provides a greater systemic half-life (t_(1/2)) of the prostacyclin compound or its treprostinil metabolite, compared to the systemic elimination half-life (t_(1/2)) of treprostinil, wrhen treprostinil is administered to the patient. In a further embodiment, administration of the prostacyclin compound and treprostinil comprises oral, nasal, subcutaneous or intravenous administration,

In another embodiment, the prostacyclin compound administered to a patient in need of PH, PAH or PPH treatment provides a greater mean pulmonary C_(max) and/or lower plasma C_(max) of treprostinil for the patient, compared to the respective pulmonary or plasma C_(max) of treprostinil, when treprostinil is administered to the patient. In a further embodiment, administration of the prostacyclin compound and treprostinil comprises intravenous administration.

In another embodiment, the prostacyclin compound administered to a patient in need of PH, PAH or PRO treatment provides a greater mean pulmonary or plasma area under the curve (AUC_(0-t)) of the prostacyclin compound or its treprostinil metabolite, compared to the mean pulmonary or plasma area under the curve (AUC_(0-t)) of treprostinil, when treprostinil is administered to the patient. In yet another embodiment, the prostacyclin compound administered to a patient in need thereof provides a greater pulmonary or plasma time to peak concentration (t_(max)) of treprostinil, compared to the pulmonary or plasma time to peak concentration (t_(max)) of treprostinil, when treprostinil is administered to the patient.

In another aspect of the invention, a method of treating a disease, disorder or condition other than PH, PAH or PPH is provided. U.S. Pat. No. 5,153,222, incorporated by reference herein in its entirety, describes use of treprostinil for treatment of pulmonary hypertension. Treprostinil is approved for the intravenous as well as subcutaneous route, the latter avoiding potential septic events associated with continuous intravenous catheters. U.S. Pat. Nos. 6,521,212 and 6,756,033, each incorporated by reference herein in their entireties, describe administration of treprostinil by inhalation for treatment of pulmonary hypertension, peripheral vascular disease and other diseases and conditions. U.S. Pat. No. 6,803,386, incorporated by reference herein in its entirety, discloses administration of treprostinil for treating cancer such lung, liver, brain, pancreatic, kidney, prostate, breast, colon and head-neck cancer. U.S. Patent Application Publication No. 2005/0165111, incorporated by reference herein in its entirety, discloses treprostinil treatment of ischemic lesions. U.S. Pat. No. 7,199,157, incorporated by reference herein in its entirety, discloses that treprostinil treatment improves kidney functions. U.S. Pat. No. 7,879,909, incorporated by reference herein in its entirety, discloses treprostinil treatment of neuropathic foot ulcers. U.S. Patent Application Publication No. 2008/0280986, incorporated by reference herein in its entirety, discloses treprostinil treatment of pulmonary fibrosis, interstitial lung disease with treprostinil and asthma. U.S. Pat. No. 6,054,486, incorporated by reference herein in its entirety, discloses treatment of peripheral vascular disease with treprostinil. U.S. patent application publication no. 2009/0036465, incorporated by reference herein in its entirety, discloses combination therapies comprising treprostinil. U.S. Patent Application Publication No. 2008/0200449 discloses delivery of treprostinil using a metered dose inhaler. U.S. Pat. Nos. 7,417,070, 7,384,978 and 7,544,713 as well as U.S. Patent Application Publication Nos. 2007/0078095, 2005/0282901, and 2008/0249167, each incorporated by reference herein in their entireties, describe oral formulations of treprostinil and other prostacyclin analogs as well as their use for treatment of a variety of conditions. U.S. Patent Application Publication No. 2012/0004307, incorporated by reference herein, discloses the use of orally administered treprostinil for treatment of Raynaud's phenomenon, systemic sclerosis and digital ischemic lesions. Each of the indications recited above can be treated with the compounds and compositions provided herein. Routes of administration to a patient in need of treatment include pulmonary (inhalation), subcutaneous, oral, nasal and intravenous.

Additionally, the following references are incorporated by reference in their entireties for ail purposes for practicing the embodiments of the present invention: J. Org. Chem. 2004, 69, 1890-1902, Drug of the Future, 2001, 26(4), 364-374, U.S. Pat. Nos. 5,153,222, 6,054,486, 6,521,212, 6,756,033, 6,803,386, and 7,199,157, U.S. Patent Application Publication Nos. 2005/0165111, 2005/0282903, 2008/0200449, 2008/0280986, 2009/0036465 and 2012/0010159.

In one embodiment, a method is provided for treating a patient in need thereof for congestive heart failure, peripheral vascular disease, asthma, severe intermittent claudication, immunosuppression, proliferative diseases, e.g., cancer such as lung, liver, brain, pancreatic, kidney, prostate, breast, colon and head-neck cancer, ischemic lesions, neuropathic foot ulcers, and pulmonary fibrosis, kidney function and/or interstitial lung disease. In one embodiment, the method comprises administering aneffective amount of one of the prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III) to the patient. Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), subcutaneous, oral, nasal or intravenous. In some embodiments, the pharmaceutical formulation may comprise one or more active ingredients in addition to treprostinil monohydrate.

In one embodiment, a method is provided for treating and/or preventing interstitial lung disease (e.g., pulmonary fibrosis) or asthma, or a condition associated with interstitial lung disease or asthma in a patient in need of such treatment. In a further embodiment, the method comprises administering to the patient an effective amount of one of the prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III). The composition or compound, in one embodiment, is delivered via a MDI by the use of a propellant, for example, a chloro-fluorocarbon (CFC) or a fluorocarbon. The patient, in one embodiment, is administered the prostacyclin compound or composition of the invention once daily, twice daily or three times daily. In one embodiment, the administration is with food. In one embodiment, each administration comprises 1 to 5 doses (puffs) from an MDI, for example 1 dose (1 puff), 2 dose (2 puffs), 3 doses (3 puffs), 4 doses (4 puffs) or 5 doses (5 puffs). The MDI, in one embodiment, is small and transportable by the patient. In another embodiment, administration is oral, nasal, subcutaneous or intravenous. In another embodiment, oral, nasal, intravenous, subcutaneous or inhalation administration of the effective amount of the prostacyclin compound or composition of the invention, for the treatment of interstitial lung disease (e.g., pulmonary fibrosis) or asthma, or a condition associated with interstitial lung disease or asthma, compared to oral, nasal, subcutaneous, intravenous or inhalation administration of treprostinil, results in a reduced severity of a systemic adverse events, or a decreased occurrence of a systemic adverse event.

In one embodiment, a method for treating an ischemic disease or condition, such as scleroderma, including systemic sclerosis, or Raynaud's Phenomenon in a patient in need of such treatment is provided. In a further embodiment, the method comprises administering an effective amount of one of the prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), to the patient. Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), oral, nasal subcutaneous or intravenous administration. In another embodiment, oral, nasal, intravenous, subcutaneous or inhalation administration of an effective amount of the prostacyclin compound or composition of the invention, for the treatment of ischemic disease or condition, such as scleroderma, including systemic sclerosis, or Raynaud's Phenomenon, compared to oral, nasal, subcutaneous, intravenous or inhalation administration of treprostinil, results in a reduced severity of a systemic adverse events, or a decreased occurrence of a systemic adverse event.

The prostacyclin compounds or compositions provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), in one embodiment, are used for treating a patient for a digital ischemic lesion, such as a digital ulcer or a necrotic lesion, or for ameliorating a symptom or functional deficit and/or reducing the number of symptoms and/or functional deflcit(s) associated with a digital ischemic lesion. The term “digital ischemic lesion” refers to a lesion on a digit, i.e., a toe or a finger, of a subject, such as a human being. In one embodiment, the digital ischemic lesion may be caused by or associated with an ischemic disease or condition, such as scleroderma, including systemic sclerosis, or Raynaud's Phenomenon. The symptom that may be ameliorated and/or reduced may be, for example, a pain associated with a digital ischemic ulcer and/or scleroderma. In some embodiments, administering a prostacyclin compound or composition provided herein, upon administration to a patient in need of treatment, provides amelioration or reduction of one or more functional deficits associated with a digital ischemic lesion. For example, in one embodiment, the prostacyclin compound or composition provided herein ameliorates or reduces a hand function deficit, i.e., provides an improvement in the hand function of the treated patient. Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), oral, nasal, subcutaneous or intravenous administration. In another embodiment, oral, nasal intravenous, subcutaneous or inhalation administration of an effective amount of the prostacyclin compound or composition of the invention, for the treatment of digital ischemic lesions, compared to oral, nasal, subcutaneous, intravenous or inhalation administration of treprostinil, results in a reduced severity of a systemic adverse events, or a decreased occurrence of a systemic adverse event,

In one embodiment, a method for improving kidney function or treating symptoms associated with kidney malfunction or failure in a patient in need thereof is provided. In a further embodiment, the method comprises administering to a subject in need thereof an effective amount of a prostacyclin compound or composition provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), to the patient. Specific symptoms associated with reduced kidney functions include, for example, abnormally low urination, increased blood levels of creatinine and urea nitrogen, protein leakage in urine and/or pain. Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), oral, nasal, subcutaneous or intravenous administration. In another embodiment, oral, nasal, intravenous, subcutaneous or inhalation administration of an effective amount of the prostacyclin compound or composition of the invention, for improvement of kidney functions or amelioration of symptoms associated with kidney malfunction or failure, compared to oral, nasal, intravenous, subcutaneous or inhalation administration of treprostinil, results in a reduced severity of a systemic adverse events, or a decreased occurrence of a systemic adverse event.

In one embodiment, a method of treating a cardiovascular disease including congestive heart failure comprises is provided. The method, in one embodiment, comprises administering to a patient in need thereof, a prostacyclin compound or composition provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof; or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III). Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), subcutaneous, oral, nasal or intravenous administration.

In one embodiment, a method for treating a peripheral vascular disease, including peripheral arterial occlusive disease and intermittent claudication is provided. In one embodiment, the method comprises administering to a patient in need thereof a prostacyclin compound or composition provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III). In addition to the prostacyclin compounds and compositions provided herein, other pharmacologically active substances may be present in the formulations of the present invention which are known to be useful for treating peripheral vascular disease. For example, the compounds of the invention may be present in combination with trental, a substance known to increase red blood cell deformability. Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), subcutaneous, oral, nasal or intravenous administration.

In one embodiment, a method for treating and/or preventing neuropathic diabetic foot ulcer is provided. In one embodiment, the method comprises administering to a patient in need thereof, a prostacyclin compound or composition provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a composition comprising a deuterated compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III). Administration, in one embodiment, is via inhalation (e.g., with a nebulizer or metered dose inhaler), subcutaneous, oral, nasal or intravenous administration. In addition to the prostacyclin compounds and compositions provided herein, other pharmacologically active substances may be present in the formulations of the present invention which are known to be useful for treating and/or preventing foot ulcers in patients with diabetic neuropathy. For example, the compounds of the invention may be present in combination with analgesics to treat pain, dressing changes, vasodilator medications, and topical or oral antibiotics.

In one embodiment, administration of an effective amount of a prostacyclin compound or composition of the present invention for the treatment of the various diseases and indications described throughout, by inhalation, subcutaneous, oral, nasal or intravenous administration, results in a decreased number of side effects, or a reduced severity of one or more side effects (also referred to herein as “adverse events”), compared to the administration of an effective amount of treprostinil, when an effective amount of treprostinil is administered by inhalation, subcutaneous, oral, nasal or intravenous administration. For example, in one embodiment, a patient treated by the methods provided herein experiences a reduced severity and/or frequency in cough or a reduced cough response when administered a prostacylin compound or composition of the invention via inhalation (e.g., nebulization, dry powder inhaler, or via a metered dose inhaler), compared to the severity and/or frequency of cough or cough response elicited by inhalation administration of treprostinil to the patient.

In another embodiment, the prostacyclin compound administered to a patient in need of treatment provides a greater mean pulmonary Cmax and/or lower plasma C_(max) of treprostmil for the patient, compared to the respective pulmonary or plasma C_(max) of treprostinil, when treprostinil is administered to the patient.. In a further embodiment, administration of the prostacyclin compound and treprostinil comprises intravenous administration.

In another embodiment, the prostacyclin compound administered to a patient in need of treatment provides a greater mean pulmonary or plasma area under the curve (AUC_(0-t)) of the prostacyclin compound or its treprostinil metabolite, compared to the mean pulmonary or plasma area under the curve (AUC_(0-t)) of treprostinil, when treprostlnil is administered to the patient. In yet another embodiment, the prostacyclin compound admini stered to a patient in need thereof pro vides a greater pulmonary or plasma time to peak concentration (t_(max)) of treprostinil, compared to the pulmonary or plasma time to peak concentration (t_(max)) of treprostinil, when treprostinil is administered to the patient.

In one embodiment, a prostacyclin compound or composition provided herein, for example, a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, or a composition comprising a compound of Formula (I), (Ia), (Ib), (Ic), (Id), (Ia′), (Ib′), (Ic′), (Id′), (Ia″), (Ib″), (Ic″), (Id″), (II), (IIa), (IIb), (IIc) (IId), or (III), or a deuterated version thereof, is administered in combination with one or more additional active agents. In some embodiments, such one or more additional active agents can be also administered together with a prostacyclin compound or composition provided herein using a metered dose inhaler. In one embodiment, such one or more additional active agents can be administered separately, i.e., prior to, or subsequent to, the prostacyclin compound or composition provided herein. Particular additional active agents that can be administered in combination with treprostinil may depend on a particular disease or condition for treatment or prevention of which treprostinil is administered. In some cases, the additional active agent can be a cardiovascular agent such as a cox-2 inhibitor, a rho kinase inhibitor, a calcium channel blocker, a phosphodiesterase inhibitor, an endothelial antagonist, or an antiplatelet agent.

As provided above, the prostacyclin compounds and compositions of the present invention can be delivered to a patient in need thereof via an oral, nasal, pulmonary , intravenous or subcutaneous route. With respect to the pulmonary route, the prostacyclin compounds and compositions) of the present invention may be used in any dosage dispensing device adapted for such administration. The device, in one embodiment, is constructed to ascertain optimum metering accuracy and compatibility of its constructive elements, such as container, valve and actuator with the formulation and could be based on a mechanical pump system, e.g., that of a metered-dose nebulizer, dry powder inhaler, soft mist inhaler, or a nebulizer. For example, pulmonary delivery devices include a jet nebulizer, electronic nebulizer, a soft mist inhaler, and a capsule-based dry powder inhaler.

Suitable propellants, e.g., for MDI delivery, may be selected among such gases as fluorocarbons, chlorofluorocarbons (CFCs), hydrocarbons, hydrofluoroalkane propellants (e.g., HFA-134a and HFA-227), nitrogen and dinitrogen oxide or mixtures thereof.

The inhalation delivery device can be a nebulizer, dry powder inhaler, or a metered dose inhaler (MDI), or any other suitable inhalation delivery device known to one of ordinary skill in the art. The device can contain and be used to deliver a single dose of the prostacyclin composition or the device can contain and be used to deliver multi-doses of the composition of the present invention.

A nebulizer type inhalation delivery device can contain the compositions of the present invention as a solution, usually aqueous, or a suspension. For example, the prostacyclin compound or composition can be suspended in saline and loaded into the inhalation delivery device. In generating the nebulized spray of the compositions for inhalation, the nebulizer delivery device may be driven ultrasonically, by compressed air, by other gases, electronically or mechanically (e.g., vibrating mesh or aperture plate). Vibrating mesh nebulizers generate fine particle, low velocity aerosol, and nebulize therapeutic solutions and suspensions at a faster rate than conventional jet or ultrasonic nebulizers. Accordingly, the duration of treatment can be shortened with a vibrating mesh nebulizer, as compared to a jet or ultrasonic nebulizer. Vibrating mesh nebulizers amenable for use with the methods described herein include the Philips Respironi.cs I-Neb®, the Omron Micro Air, the Nektar Aeroneb®, and the Pari eFlow®.

The nebulizer may be portable and hand held in design, and may be equipped with a self contained electrical unit. The nebulizer device may comprise a nozzle that has two coincident outlet channels of defined aperture size through which the liquid formulation can be accelerated. This results in impaction of the two streams and atomization of the formulation. The nebulizer may use a mechanical actuator to force the liquid formulation through a multiorifice nozzle of defined aperture size(s) to produce an aerosol of the formulation for inhalation. In the design of single dose nebulizers, blister packs containing single doses of the formulation may be employed.

In the present invention the nebulizer may be employed to ensure the sizing of particles is optimal for positioning of the particle within, for example, the pulmonary membrane.

Upon nebulization, the nebulized composition (also referred to as “aerosolized composition”) is in the form of aerosolized particles. The aerosolized composition can be characterized by the particle size of the aerosol, for example, by measuring the “mass median aerodynamic diameter” or “fine particle fraction” associated with the aerosolized composition. “Mass median aerodynamic diameter” or “MM AD” is normalized regarding the aerodynamic separation of aqua aerosol droplets and is determined by impactor measurements, e.g., the Anderson Cascade Impactor (ACI) or the Next Generation Impactor (NGI). The gas flow rate, in one embodiment, is 28 Liter per minute for the ACI and 15 liter per minute for the NGI.

“Geometric standard deviation” or “GSD” is a measure of the spread of an aerodynamic particle size distribution. Low GSDs characterize a narrow droplet size distribution (homogeneously sized droplets), which is advantageous for targeting aerosol to the respiratory system. The average droplet size of the nebulized composition provided herein, in one embodiment is less than 5 μm or about 1 μm to about 5 μm, and has a GSD in a range of 1.0 to 2.2, or about 1.0 to about 2.2, or 1.5 to 2.2, or about 1.5 to about 2.2.

“Fine particle fraction” or “FPF,” as used herein, refers to the fraction of the aerosol having a particle size less than 5 μm in diameter, as measured by cascade impaction. FPF is usually expressed as a percentage.

In one embodiment, the mass median aerodynamic diameter (MMAD) of the nebulized composition is about 1 urn to about 5 pin, or about 1 urn to about 4 μm, or about 1 μm to about 3 μm or about 1 μm to about 2 μm, as measured by the Anderson Cascade Impactor (ACI) or Next Generation Impactor (NGI). In another embodiment, the MMAD of the nebulized composition is about 5 μm or less, about 4 μm or less, about 3 μm or less, about 2 μm or less, or about 1 μm or less, as measured by cascade impaction, for example, by the ACI or NGI.

In one embodiment, the MMAD of the aerosol of the pharmaceutical composition is less than about 4.9 μm, less than about 4.5 μm, less than about 4.3 μm, less than about 4.2 μm, less than about 4.1 μm, less than about 4.0 μm or less than about 3.5 μm, as measured by cascade impaction.

In one embodiment, the MM AD of the aerosol of the pharmaceutical composition is about 1.0 μm to about 5.0 μm, about 2.0 μm to about 4.5 μm, about 2.5 μm to about 4.0 μm, about 3.0 μm to about 4.0 μm or about 3.5 μm to about 4.5 μm, as measured by cascade impaction (e.g., by the ACI or NGI).

In one embodiment, the FPF of the aerosolized composition is greater than or equal to about 50%, as measured by the ACI or NGI, greater than or equal to about 60%, as measured by the ACI or NGI or greater than or equal to about 70%, as measured by the ACI or NGI. In another embodiment, the FPF of the aerosolized composition is about 50% to about 80%), or about 50% to about 70% or about 50% to about 60%, as measured by the NGI or ACI.

In one embodiment, a metered dose inhalator (MDI) is employed as the inhalation delivery device for the compositions of the present invention. In a further embodiment, the prostacyclin compound is suspended in a propellant (e.g., hydroflourocarbon) prior to loading into the MDI. The basic structure of the MDI comprises a metering valve, an actuator and a container. A propellant is used to discharge the formulation from the device. The composition may consist of particles of a defined size suspended in the pressurized propellant(s) liquid, or the composition can be in a solution or suspension of pressurized liquid propeilant(s). The propellants used are primarily atmospheric friendly hydroflourocarbons (HFCs) such as 134a. and 227. The device of the inhalation system may deliver a single dose via, e.g., a blister pack, or if. may be multi dose in design. The pressurized metered dose inhalator of the inhalation system can be breath actuated to deliver an accurate dose of the lipid-containing formulation. To insure accuracy of dosing, the delivery of the formulation may be programmed via a microprocessor to occur at a certain point in the inhalation cycle. The MDI may be portable and hand held.

In one embodiment, a dry powder inhaler (DPI) is employed as the inhalation delivery device for the compositions of the present invention. In one embodiment, the DPI generates particles having an MM AD of from about 1 μm to about 10 μm, or about 1 μm to about 9 μm, or about 1 μm to about 8 μm, or about 1 μm to about 7 μm, or about 1 μm to about 6 μm, or about 1 μm to about 5 μm, or about 1 μm to about 4 μm, or about 1 μm to about 3 μm, or about 1 μm to about 2 μm in diameter, as measured by the NGI or ACI. In another embodiment, the DPI generates a particles having an MMAD of from about 1 μm to about 10 μm, or about 2 μm to about 10 μm, or about 3 urn to about 10 μm, or about 4 μm to about 10 μm, or about 5 μm to about 10 μm, or about 6 μm to about 10 μm, or about 7 μm to about 10 μm, or about 8 μm to about 10 μm, or about 9 μm to about 10 μm, as measured by the NGI or ACI.

In one embodiment, the MMAD of the particles generated by the DPI is about 1 μm or less, about 9 μm or less, about 8 μm or less, about 7 μm or less, 6 μm or less, 5 μm or less, about 4 μm or less, about 3 μm or less, about 2 μm or less, or about 1 μm or less, as measured by the NGI or ACI.

In one embodiment, the MMAD of the particles generated by the DPI is less than about 9.9 μm, less than about 9.5 μm, less than about 9.3 μm, less than about 9.2 μm, less than about 9.1 μm, less than about 9.0 μm, less than about 8.5 μm, less than about 8.3 μm, less than about 8.2 μm, less than about 8.1 μm, less than about 8,0 μm, less than about 7.5 μm, less than about 7.3 μm, less than about 7.2 μm, less than about 7.1 μm, less than about 7.0 μm, less than about 6.5 μm, less than about 6.3 μm, less than about 6.2 μm, less than about 6.1 μm, less than about 6.0 μm, less than about 5.5 μm, less than about 5.3 μm, less than about 5.2 μm, less than about 5.1 μm, less than about 5.0 μm, less than about 4,5 μm, less than about 4.3 μm, less than about 4.2 μm, less than about 4.1 μm, less than about 4.0 μm or less than about 3.5 μm, as measured by the NGI or ACI.

In one embodiment, the MMAD of the particles generated by the DPI is about 1.0 μm to about 10.0 μm, about 2.0 μm to about 9.5 μm, about 2.5 μm to about 9.0 μm, about 3.0 μm to about 9.0 μm, about 3.5 μm to about 8.5 μm or about 4.0 μm to about 8.0 μm.

In one embodiment, the FPF of the prostacyclin particulate composition generated by the DPI is greater than or equal to about 40%, as measured by the ACI or NGI, greater than or equal to about 50%, as measured by the ACI or NGI, greater than or equal to about 60%, as measured by the ACI or NGI, or greater than or equal to about 70%, as measured by the ACI or NGI. In another embodiment, the FPF of the aerosolized composition is about 40% to about 70%, or about 50% to about 70% or about 40% to about 60%, as measured by the NGI or ACI.

EXAMPLES

The present invention is further illustrated by reference to the following Examples, However, it should be noted that these Examples, like the embodiments described above, are illustrative and are not to be construed as restricting the scope of the invention in any way.

Example 1 Synthesis of Treprostinil Alkyl Esters

Treprostinil compounds derivatized with alkyl groups at the carboxylic acid moiety were prepared. Specifically, treprostinil was derivatized at the carboxylic acid moiety with C₂, C₃, C₄, C₅, C₆, C₈, C₁₀, C₁₂, C₂₆, and C₁₈ alkyl chains (i.e., R₂ in Formula (A), below, is C₂, C₃, C₄, C₅, C₆, C₈, C₁₀, C₁₂, C₁₆ or C₁₈ alkyl) to make treprostinil alkyl esters of various ester chain lengths, Treprostinil can be synthesized, for example, by the methods disclosed in U.S. Pat. Nos. 6,765,117 and 8,497,393. Synthesis of prostaglandin derivatives is described in U.S. Pat. No, 4,668,814. The disclosures of U.S. Pat. Nos. 6,765,117; 8,497,393 and 4,668,814 are each incorporated by reference in their entireties for all purposes.

Scheme 1:

Treprostinil esterifieation was catalyzed by strongly acidic resin Amberlyst® 15 (Rohm and Haas). Treprostinil acid was dissolved in anhydrous dioxane/alcohol at a concentration 10 mg/mL (typically 4 mL). Alcohol (R₂—OH) added was appropriate to make corresponding chain length at the R₂ group. By way of example, for the C₂ (ethyl ester) compound, the alcohol was ethanol. The molar amount of alcohol in the solvent was ten times the molar amount of treprostinil.

Treprostinil in dioxane/alcohol solution was added to washed and dry Amberlyst resin. Per each 40 mg treprostinil, 1 g resin in a glass vial was added. The mixture was placed on a shaker and incubated overnight at 40° C. Next, the liquid portion was taken out of the vial, washed twice with 3 mL dioxane. All recovered solvent was then collected. The solvent was dried by nitrogen stream until the evaporation stopped. The remaining treprostinil alkyl ester and nonvolatile alcohol (if long chain alcohol used) was dissolved in 2 mL hexane/ethyl acetate 1:1, and cleaned by liquid-liquid extraction vs. equal volume of phosphate buffer, and then water. Next, the organic layer was separated and dried by nitrogen stream and further in vacuum. If a long chain alcohol used, an additional purification step was required to separate alcohol by liquid chromatography. ACE CN, 5 μm, Ultra-Inert HPLC Column, 100×21.2 mm was used, with mobile phase of hexane/propanol 98:2%.

Scheme 2:

To a solution of (1R,2R,3aS,9aS)-[[2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3S)-3-hydroxyoctyl]-1H-benz[f]inden-5-yl]oxy]acetic acid (treprostinil) (78.1 mg, 200 μmoles) dissolved in 1,4-dioxane (2.0 ml.) was added Amberlyst® 15 resin (2.0 g) and alcohol R₂—OH (2.0 mmoles, 10 equivalents). The reaction mixture was heated to 40° C. and allowed to shake at approximately 100 rpm for 18-196 hours. Solvent was removed and the resin was washed with acetonitrile (MeCN) (3×3 mL). The 1,4-dioxane and MeCN extracts were combined and dried using a gentle stream of warmed N₂ gas and gentle heat to yleld a thick waxy solid. The crude material was dissolved in 20% ^(n)PrOH/Hexanes and submitted to preparatory HPLC purification. Solvent was removed from the purified material using a gentle stream of warmed N₂ gas and gentle heat to yleld an off-white waxy solid. The pure material was suspended in ethyl lactate for storage and was submitted to analytical HPLC for concentration determination.

By way of example, the following compounds of Formula (A) were synthesized by the method of scheme 2.

Compound R₂ group abbreviation

C₁₆-TR

C₁₄-TR

C₁₂-TR

C₁₀-TR

C₉-TR

5C₉-TR

2C₉-TR

(S)-2C₉-TR

(R)-2C₉-TR

C₈-TR

(S)-2C₈-TR

(R)-2C₈-TR

3C₈-TR

4C₈-TR

C₆-TR

C₅-TR

C₄-TR

C₃-TR

C₂-TR

A general diagram for synthesis of the ethyl ester of treprostinil is shown in Scheme 1, below. The alcohol can be modified based on the desired alkyl ester chain length (e.g., C₅-C₁₈ alkyl esters of even or odd chain length, straight chain or branched).

Example 2 Spontaneous and Esterase-Mediated Hydrolysis of Treprostinil Alkyl Esters

Spontaneous and/or esterase-mediated hydrolysis was measured for the prostacyclin alkyl ester compositions provided in Table 2. Cx indicates the alkyl chain length at position R₂ of the compound of Formula (A), provided above.

TABLE 2 Components of prostacyclin alkyl ester compositions Hydrophobic Cx- Hydrophobic PEGylated Cx-TR Additive PEG-lipid DOPC Composition TR Additive lipid mol % mol % mol % mol % T493 C₂-TR Squalane Chol- 40 40 20 0 PEG2k T500 C₄-TR Squalane Chol- 40 40 20 0 PEG2k T507 C₆-TR Squalane Chol- 40 40 20 0 PEG2k T508 C₈-TR Squalane Chol- 40 40 20 0 PEG2k T509 C₁₀- Squalane Chol- 40 40 20 0 TR PEG2k T554 C₂-TR Squalane Chol- 40 40 10 10 PEG2k T555 C₈-TR Squalane Chol- 40 40 10 10 PEG2k T556 C₁₀- Squalane Chol- 40 40 10 10 TR PEG2k T568 C₁₂- Squalane Chol- 40 40 10 10 TR PEG2k T623 C₁₆- Squalane Chol- 40 40 10 10 TR PEG2k T637 C₁₈- Squalane Chol- 40 40 10 10 TR PEG2k

Additionally, spontaneous hydrolysis was measured for 200 μM of treprostinil compounds derivatized at the carboxylic acid group with either a C₃, C₄, C₅, C₆, C₈ or C₁₀ alkyl group in 20% ethanol at 40° C. at six time points (0 hr., 1 hr., 2 hr., 4 hr., 6 hr., 24 hr.).

Each sample was prepared as a 200 μM solution in 20% ethanol. At each time point, an aliquot was removed for HPLC analysis to resolve remaining reaetants (C₃, C₄, C₅, C₆, C₈, C₁₀) or their degradation product (treprostinil). For each sample, hydrolysis was calculated from the measured reactant and product peak areas:

% hydrolysis−(product peak area/(reactant peak area+product peak area)*100).

The results of the time course experiment are provided at FIG. 1A, The results indicate that hydrolysis rate is correlated with the length of the alkyl ester moiety.

Esterase mediated hydrolysis of treprostini l compounds and compositions was measured for compounds derivatized at the carboxylic acid group with C₂, C₄, C₆, C₈ and C₁₀ alkyl groups and compositions comprising the same. Experiments were conducted at 37° C., and hydrolysis was measured at 15 min., 30 min., and 1 hour after addition of the esterase to the compound solution. The reaction mixture for each sample was prepared at a final volume of 500 μL containing, 200 μM treprostinil compound, 0.05 U esterase, 20% ethanol, and PBS. Hydrolysis was measured as described above.

The results of this experiment are provided at FIG. 1B. The results indicate that compound degradation rate decreases with increasing alkyl ester chain length.

Treprostinil alkyl ester conversion to treprostinil was also measured in the presence of rat, dog and monkey lung tissue homogenate at 37° C. Mere, data were calculated based on fit of exponential increase to the maximum (experiments performed in duplicate). The results of this study are provided below in Table 2A and FIG. 37. Specifically, FIG. 37 left, shows that conversion to treprostinil depends on alkyl chain length. In this experiment, treprostinil alkyl esters were incubated for 4 hours at a final concentration of 200 nM in 1 mL of tissue homogenate prepared in water and normalized to 10 mg/mL of protein.

FIG. 37 right, shows conversion of C₁₂-TR to treprostinil (percentage) in the presence of rat, dog or monkey lung tissue homogenate. C₁₂-TR was incubated for 4 hours at a final concentration of 200 nM in 1 mL of tissue homogenate prepared in water and normalized to 10 mg/mL of protein. Both FIG. 37 experiments (left and right graphs) were performed in duplicate and the lines represent nonlinear exponential regression assuming 1 phase decay.

TABLE 2A Rate of treprostinil alkyl ester conversion in the presence of rat, dog or monkey lung tissue homogenate. Rate of treprostinil alkyl ester conversion (nmOL/h * g of protein) C₈-TR C₁₀-TR C₁₂-TR C₁₄-TR Rat 32.5 7.3 1.1 0.4 Dog 49.8 10.5 2.2 — Monkey 17.3 4.6 0.6 —

Example 3 Particle Size Characterization of Treprostinil Compositions

The compositions in Table 3 were subject to particle size characterization. Cx indicates the alkyl chain length at position R₂ of Formula (A), provided above.

TABLE 3 Compositions subject to particle size characterization Hydrophobic PEGylated Hydrophobic PEGylated Cx-TR Additive lipid DOPC Composition Cx-TR Additive lipid mol % mol % mol % mol % T554 (C₂) C₂-TR Squalane Chol- 40 40 10 10 PEG2k T499 (C₃) C₃-TR Squalane Chol- 40 40 20 0 PEG2k T500 (C₄) C₄-TR Squalane Chol- 40 40 20 0 PEG2k T501 (C₅) C₅-TR Squalane Chol- 40 40 20 0 PEG2k T601 (C₆) C₆-TR Squalane Chol- 40 40 10 10 PEG2k T555 (C₈) C₈-TR Squalane Chol- 40 40 10 10 PEG2k T556 (C₁₀) C₁₀-TR Squalane Chol- 40 40 10 10 PEG2k T568 (C₁₂) C₁₂-TR Squalane Chol- 40 40 10 10 PEG2k T623 (C₁₆) C₁₆-TR Squalane Chol- 40 40 10 10 PEG2k T637 (C₁₈) C₁₈-TR Squalane Chol- 40 40 10 10 PEG2k

All particle size measurements were performed using a Wyatt Technology Mobius™ Zeta Potential/ Particle Sizing Instrument in Quasi-elastic light scattering (QELS) mode. Composition aiiquots were diluted 10-fold in pre-filtered (0.02 μm pore filter) ultrapure of deionized H₂O. Light scattering data was collected and converted into particle size and size distribution using Dynamics® v. 7.2.4 instrument software. Reported average particle size diameter is based on the cumulants model, which mathematically fits particle diffusion constants (determined by the raw scattering intensities of particles in a suspension) to obtain the particle size mean and a distribution of particle sizes around the mean diameter.

It was found that the particle size (average particle diameter) of treprostinil compositions increases in size in compositions comprising C₂-C₅ alkyl ester derivatized treprostinil, and decreases in size in compositions comprising C₆-C₁₂ alkyl ester derivatized treprostinil. These results are provided in FIG. 2. The largest average particle diameter was found for compositions comprising treprostinil pentyl ester (i.e., treprostinil derivatized with a C₅ alkyl ester) (316 nm). Compositions comprising treprostinil ethyl ester had an average particle diameter of 41 nm. It should be recognized that through manipulation of processing parameters the same compositions could be produced with different mean diameters and size distributions. Manipulations of composition in combination with manipulation of processing parameters could also be performed to produce particles of various sizes.

Under the conditions utilized here it was also found that longer chain derivatized treprostinil compounds formed more uniform particles than compounds having shorter alkyl ester chains. Particle uniformity was determined using the software-calculated polydispersity (% PD). Polydispersity is defined as the standard deviation of the particle size distribution from the mean particle size value. % PD normalizes the polydispersity to the mean diameter by dividing by the mean size and multiplylng by 100. These parameters indicate whether a particle suspension has one or more size populations of particles (monomodal versus multimodal). It also gives insight into the width of particle size distribution (or degree particle uniformity) around the mean for the respective particle populations.

Dynamics® polydispersity parameter represents a monodisperse population of particles if % PD≦15. A calculated % PD≧57% represents a polydisperse population of particles. For instance, the %PD data plotted in FIG. 2 ylelds information about the uniformity of particle size populations from the treprostinil compounds tested. C₈-TR (TR=treprostinil), C₁₀-TR, C₁₂-TR, and C₁₄-TR alkyl esters ylelded near monodisperse particles with % PD at or around 15. C₂-TR, C₆-TR, C₁₆-TR, and C₁₈-TR alkyl esters ylelded particles that have % PD slightly above the 15, suggesting that there is one population of particles. However, these particles possessed a wider distribution of particles sizes around the mean particle size when compared to C₈-TR, C₁₀-TR, C₁₂-TR, and C₁₄-TR. C₃-TR, C₄-TR, and C₅-TR showed much greater than 15 % PD and some ≧57. These values indicate that there are multiple populations of particles that possess wide particle size distributions.

Example 4 Measurement of Cyclic Adenosine Monophosphate (cAMP) Levels in CHO—K1 Cells in Response to Treprostinil Compositions

A cell based Chinese hamster ovary-K1 (CHO—KT) assay based on the GloSensor™ cAMP assay (Promega) was used to characterize the effect of treprostinil alkyl ester compounds on cAMP levels.

cAMP is a second messenger involved in signal transduction of G-protein coupled receptors (GPCRs) acting through Ga-s and Ga-i proteins. Because the treprostinil receptor is a GPCR, the assay provides an indication of whether the respective prostacyclin compound (or metabolite thereof) binds its receptor and activates the GPCR cell signaling cascade.

The GloSensor™ assay harnesses a genetically modified form of firefly luciferase into which a cAMP-binding protein moiety has been inserted. Upon binding of cAMP, a conformational change is induced leading to increased light output.

The EP2 prostanoid receptor was co-transfected with the GloSensor™ plasmid (Promega) into CHG-K1 cells as follows. CHO—K1 cells were harvested when the monoloayer was at 50-90% confluence. First, cells were washed with 5 mL PBS. Two ml of pre-warmed (37° C) 0.05% trypsin-EDTA (Life Technologies, Cat #: 25300054) was added, and cells were dislodged by tapping the flask on the side. Next, 10 mL of antibiotic free growth media (Life Tech, Cat #: 31765092) containing 10% fetal bovine serum (FBS; Hyclone, Cat #: SH30071.03) was added, and cells were centrifuged at 250×g for 5 minutes at room temperature. The media was aspirated, and the cell pellet was resuspended in 10 mL of growth media. Cell number was determined using a hemacytometer. Each well of a culture treated 96 wrell flat bottom plate (Costar, Cat #: 3917) was seeded with 1×10⁴ cells per 100 μL antibiotic-free growth media. The cells were incubated overnight at 37° C and 5% CO₂ in a water-jacketed incubator.

For small scale transfections of up to 20 wells, the pGLoSensor-22F cAMP plasmid (Promega, Cat #: E2301) (2 μg): (EP2) (10 ng) (Origene, Cat #: SC₁₂₆₅₅₈) : pGEM-3Zf(+) (10 ng) (Promega, Cat #: P2271) ratio was diluted to a final concentration of 12.6 ng/μL (total plasmid) in Opti-MEM I reduced-serum medium (Life Technologies, Cat #: 1985062). Next, 6 μL of FuGENE HD transfection reagent (Promega, Cat #: E2311) was

added to 160 μL of diluted plasmid and mixed carefully by gentle pipetting. The complex was incubated at room temperature for 0 to 10 minutes, and then 8 μL of the complex was added per well of a 96 well white assay plate (Costar, Cat #: 3917) and gently mixed without disturbing the cell monolayer. The plates were incubated for 20-24 hours at 37° C. and 5% CO₂ in a water-jacketed incubator. Following incubation, cells were treated and analyzed.

For larger scale transfections, the aforementioned steps were scaled up accordingly, and cells were frozen following the last incubation. In order to prepare frozen transfected CHO—K1 cells, the media was aspirated from culture flasks and cells were rinsed with 5 mL PBS. As above, 2 mL of pre-warmed (37° C.) 0.05% trypsin-EDTA (Life Technologies, Cat #: 25300054) was added, and cells were dislodged by tapping the flask on the side. Next, 10 mL of antibiotic free growth media (Life Technologies, Cat #: 31765092) containing 10% FBS (Hyclone, Cat #: SH30071.03) was added, and cells were centrifuged at 250×g for 5 minutes at room temperature. Cell number was determined using a hemacytometer. The media was aspirated, and the cell pellet was resuspended in freezing media (Millipore, cat #: S-002-5F) at 2.5×10⁶ cells/vial. Transfected cells were incubated overnight at −80° C. before transfer to liquid nitrogen for long term storage. The frozen stocks were then thawed one day prior to use for assays, and cells were seeded at 2.5×10⁴ cells per well in 100 μL of antibiotic-free complete media (F12 (Life Technologies, Cat #: 31765092) +10% FBS (Hyclone, Cat #: SH30071.03)). Following an overnight incubation at 37° C. and 5% CO₂ in a water-jacketed incubator, the cells were ready for use in cAMP response assays.

In preparation for cAMP measurement, the cells were equilibrated with the GloSensor cAMP reagent prior to treatment. For equilibration, the medium was carefully removed from the individual well. Next, 100 μL of equilibration medium (6% v/v of Glosensor Reagent stock solution (Promega, Cat #: E291), 10% FBS (Hyclone, Cat #: SH30071.03) and 88% CO₂ independent medium (Life Technologies, Cat #: 18045088)) was added per well of the 96-well plate, and added to the side of each well. The plate was then incubated for 2 hours at room temperature. A first pre-read measurement was taken using a microplate reader (MicroLumat Plus). Plates were incubated for an additional 10 minutes at room temperature, followed by a second pre-read measurement.

Working solutions of free treprostinil and treprostinil alkyl ester compounds were prepared at 10× concentration so that the final concentration was 1× once added to the cells. Following treatment, each plate was read every 5 minutes for the duration of the assay using a microplate reader (MicroLumat Plus). In order to determine the fold change in cAMP relative to the control, the transfection efficiency was first determined by dividing the second pre-read measurement by the average of the corresponding pre-read measurements. Next, the normalized relative light units (RLUs) of the samples were determined by dividing the plate read measurement by the transfection efficiency. The fold change in cAMP relative to the control was then determined by dividing the normalized RLU of the samples by the normalized RLU of the control.

Validation of cAMP Assay Using Free Treprostinil

The cAMP assay was validated using free treprostinil. Treprostinil (10 μM, 1 μM, 0.1 μM, 0.01 μM, 0.001 μM, 0.0001 μM, 0.00001 μM, and 0.000001 μM) was added to equilibrated CHO—K1 cells, and the cells were then incubated for 30 minutes. Luminescence was then measured at room temperature.

Alkyl Ester Treprostinil Compositions

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with free treprostinil (10 μM, 1 μM, 0.1 μM, 0.01 μM, 0.001 μM, 0.0001 μM, 0.00001 μM, 0.000001 μM) and treprostinil alkyl ester compounds, i.e., compounds having either a C₆, C₈ or C₁₀ straight chain alkyl group at the R₂ position of the compound of Formula (A), shown above.

The following concentrations of compounds were measured: 10 μM, 1 μM, 0.1 μM, 0.01 μM, 0.001 μM, 0.0001 μM, 0.00001 μM, 0.000001 μM. cAMP levels were then measured every 5 minutes over a time course of 8 hours. Results from the three highest concentrations are provided at FIG. 3A (10 μM), FIG. 3B (1 μM) and FIG. 3C (0.1 μM). The components of the treprostinil compositions set forth in FIGS. 3A, 3B and 3C are shown in Table 4 below.

cAMP levels in response to the treprostinil decyl ester (C₁₀-TR) (10 μM) were equivalent to free treprostinil and the levels were sustained for at least 6 hours. The sustained cAMP level was not exhibited in response to free treprostinil.

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with free treprostinil (5 μM) and treprostinil compositions having either a treprostinil derivatized at the R₂ position of the above compound with a C₂, C₆, C₈, C₁₀, or C₁₂ straight chain group (5 μM). The components of the treprostinil compositions are provided in Table 5, below. cAMP levels were then measured every 5 minutes over a time course of 8 hours.

Results of these experiments using the 5 μM dose are provided at FIG. 4 and FIG. 5. cAMP response to the C₂ and C₁₀ treprostinil alkyl esters (5 μM) was greater than or equivalent to the response induced by free treprostinil (FIG. 4). The cAMP levels in response to the C₂ and C₁₀ treprostinil alkyl ester compounds were sustained significantly longer than free treprostinil and the C₆, C₈, and C₁₂ treprostinil derivatives.

TABLE 4 Treprostinil alkyl ester compositions shown in FIG. 3. Chol- Composition Cx-TR Tocoacetate PEG2000 Squalane DOPC Max cAMP level (Cx-TR) mol % mol % mol % mol % mol % (Fold) Treprostinil 100 ~16 T543 (C₆-TR) 40 40 20 0 ~8 T555 (C₈-TR) 40 10 40 10 ~14 T556 (C₁₀-TR) 40 10 40 10 ~16

TABLE 5 Treprostinil alkyl ester compositions shown in FIG. 4. Max Composition Cx- Chol- Squa- cAMP (Cx-TR) TR PEG2000 lane DOPC level (concentration) mol % mol % mol % mol % (Fold) Treprostinil 100 ~14 T554 (C₂-TR) (5 μM) 40 10 40 10 ~24 T601 (C₆-TR) (5 μM) 40 10 40 10 T555 (C₈-TR) (5 μM) 40 10 40 10 ~13 T556 (C₁₀-TR) (5 μM) 40 10 40 10 ~17 T568 (C₁₂-TR) (5 μM) 40 10 40 10 ~9

Treprostinil Compounds

The cell based (CHO—K1) cAMP assay was also used to characterize the effect of unformulated treprostinil compounds (i.e., compounds without a hydrophobic additive and/or an amphiphilic agent such as a PEGylated lipid) on cAMP levels.

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with free treprostinil (5 μM) and treprostinil derivatives having either a C₂, C₃, C₄, C₅, C₆, C₈, C₁₀, or C₁₂ straight chain alkyl ester moiety (5 μM). cAMP levels were then measured every 5 minutes over a time course of 8 hours.

Results of these experiments are provided at FIG. 5. C₂ and C₁₀ treprostinil alkyl esters induced cAMP response levels equivalent to free treprostinil. The C₁₂ derivatized treprostinil compound was found to induce the smallest cAMP response.

Nebulized Treprostinil Ester Compositions

The cell based (CHO—K1) cAMP assay described above was also used to characterize the effect of nebulization of various treprostini l compositions on cAMP levels.

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid. were challenged with 10 μM free treprostinil (control or nebulized) and 10 μM treprostinil compositions comprising a compound derivatized with either a C₂, C₈, C₁₀, or C₁₂ straight chain alkyl group at position R₂ of the compound of Formula (A), provided above (control or nebulized).

The compositions tested in this experiment are provided in Table 6 below (results in FIG. 6), cAMP levels were then measured every 5 minutes over a time course of 8 hours.

Nebulizer Aeroneb Pro (Aerogen) was used to nebulize treprostinil derivative compositions. Desired volume of the formulation (usually 3 ml.,) was loaded to the mesh head of the nebulizer. The head was connected directly to the glass impinger with air-tight seal, Nebulization was carried out using factory settings until the entire sample was nebulized. After nebulization was complete, the head was disconnected; impinger capped and centrifuged 5 min at 600×g to settle the aerosol inside the impinger. The procedure provided nearly 100% yield in collecting the nebulized sample.

As shown in FIG. 6, nebulization of the derivatized treprostinil compositions did not have a deleterious effect on cAMP response levels, or duration of the response.

TABLE 6 Treprostinil Alkyl Ester Compositions: Effect of nebulization. Max Cx- Chol- cAMP (5 μM) TR PEG2000 Squalane DOPC level Cx-TR mol % mol % mol % mol % (Fold) Treprostinil 100 ~15 T554 (C₂-TR) 40 10 40 10 ~22 T555 (C₈-TR) 40 10 40 10 ~13 T556 (C₁₀-TR) 40 10 40 10 ~18 T568 (C₁₂-TR) 40 10 40 10 ~13

Comparison of Treprostinil Compounds and Compositions Comprising the Same

The half maximal effective concentrations (EC₅₀) of the various treprostinil compounds were determined using the results from the cAMP assays. Table 7 (below) summarizes the EC₅₀ data for cAMP response in CHG-K1 cells for the following compositions and compounds:

-   T554 (C₂-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T612 (C₂-TR 10 mol %, DMPE-P1K 90 mol %), -   T501 (C₅-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 20 mol %), -   T601 (C₆-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T555 (C₈-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T556 (C₁₀-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T568 (C₁₂-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T621 (C₁₂-TR 10 mol %, DPPE-P2K 90 mol %), -   T623 (C₁₆-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol % , DOPC     10 mol %,), -   T622 (C₁₈-TR 10 mol %, DPPE-P2K 90 mol %), -   C₂-TR (100 mol %), -   C₈-TR (100 mol %), -   C₁₂-TR (100 mol %) and -   free treprostinil.

A subset of the dose response curves for selected treprostinil compounds and compositions are provided in FIGS. 7-14. With free treprostinil, the potency decreases with increasing incubation time (supporting an immediate response), while all the various treprostinil compositions exhibit an increasing potency with incubation time (suggestive of a delay-release profile).

TABLE 7 EC₅₀ values for treprostinil compositions. EC₅₀ (μM) Samples 0.5 hr 1.0 hr 2.0 hr 3.0 hr 4.0 hr 4.5 hr 5.0 hr 6.0 hr 7.0 hr 8.0 hr Treprostinil 0.18 0.28 0.15 0.16 0.19 0.2 0.26 0.29 0.46 0.44 T554 (C₂-TR) 5.96 6.05 5.25 2.43 2.14 2.12 2.22 2.31 2.28 1.96 T501 (C₅-TR) 15.4 15.4 10.9 5.98 5.64 5.07 5.07 4.46 4.11 3.92 T601 (C₆-TR) ~0.0093 45.2 14.4 75.0 22.0 21.3 24.5 9.35 6.17 4.94 T555 (C₈-TR) 20.8 15.1 5.65 4.10 2.99 2.66 2.41 2.03 1.71 1.48 T556 (C₁₀-TR) ~6.83 4.94 1.69 1.80 2.20 2.09 2.34 1.78 1.51 2.20 T568 (C₁₂-TR) 12.2 8.07 6.54 4.12 3.21 3.06 2.37 2.33 2.24 2.03 T631 (C₁₄-TR) ~0.0015 ~0.0088 34.1 12.4 3.97 2.79 2.17 1.88 1.45 1.23 T623 (C₁₆-TR) 13.7 ~0.0090 42.9 24.8 5.10 4.59 3.87 2.78 1.97 1.77 C₂-TR 2.43 2.27 1.75 1.81 1.88 1.84 1.91 1.68 1.71 1.65 (constrain) C₈-TR 3.69 3.39 1.69 1.42 1.53 1.41 1.4 1.4 1.34 1.09 (constrain) C₁₂-TR 4.98 5.35 4.54 4.07 3.13 3.17 2.94 3.25 3.17 2.9 (constrain) T612 (C₂-TR) 10.0 7.08 7.9 2.23 2.76 1.54 0.88 0.44 0.41 0.28 T622 (C₁₆-TR) ~0.012 24.6 3.53 2.2 8.29 25.2 16.3 3.9 1.90 1.14 Constrain: All EC₅₀ values were generated using GraphPad Prism 5 software. For samples, C₂-TR, C₈-TR and C₁₂-TR, the data were analyzed by constraining the top and bottom parameter to a constant number corresponding to the highest and lowest value respectively, generated from the cAMP assay. *For samples T612 (C₂-TR); T622 (C₁₆-TR), because of toxicity at higher concentrations, those values were excluded from the analyses in order to generate an EC₅₀ value.

Example 5 Determination of the Effect of Treprostinil Compounds on Cell Proliferation

In order to determine any effect of treprostinil compounds on cell proliferation, cell based assays using CHO—K1 cells and rat alveolar cells (NR8383 cells) were performed.

CHQ-K1 Cells

CHG-K1 cells were harvested when the cell monolayer was 50-90% confluent (use passage 4-11). Media was aspirated out of the flask, and cells were rinsed with 2 mL of F12 media. Next, 1 mL of pre-warmed (37° C.) 0.25%o trypsin-EDTA (Life Technologies, Cat#: 25300054) was added, and cells were dislodged from the flask by tapping it on the side. Complete growth media (F12 (Life Technologies, Cat #: 31765092) +10%FBS (Hyclone, Cat #: SH30071.03)+1× Pen-Strep (Life Technologies, cat #15140-122) was then added at a volume of 10 mL. Cells were eentrifuged at 250×g for 5 minutes at room temperature, and the media was aspirated. The cell pellet was resuspended in 10 ml. complete growth media. Cell number was determined using a hemacytometer. Ceils were then seeded at 2000 cells per well of a 96-well plate in 100 μL of complete growth media. The plate was incubated overnight at 37° C. and 5% CO₂ in a water-jacketed incubator.

The next day, 80 μL of fresh complete media was added to each well, and CHO—K1 cells were challenged with treprostinil compound and composition treatments. The working solutions were prepared at 10× concentration, and following 2 fold serial dilutions, 20 μL aliquots were added per well to arrive at a final 1× concentration. Following a 48 hour incubation at 37° C. and 5% CO₂ in a water-jacketed incubator, the inhibitory effect on cell proliferation was determined. Plates were analyzed using 20 μL of Presto Blue reagent (Life Technologies, cat #: A13262) per well. The reagent was mixed, and plates were incubated for 1 hour at 37° C. and 5% CO₂ in a water-jacketed incubator. Plates were read using either a CytoFluor Series 4000 (PerSeptive BioSystems) or Synergy Neo microplate reader (BioTek) with emission λ: 590 nm and excitation λ: 560 nm. The percent inhibition was determined using the following formula: % inhibition=100%−(treated samples/control×100%).

NR₈₃₈₃ Cells

Rat alveolar NR₈₃₈₃ cells were harvested when the monolayer was 50-90% confluent (use passage 5-11). Because the NR8383 cells include both adherent and non-adherent cells, media was transferred to a 50 mL Falcon tube. To obtain the cells remaining in the flask, 2 mL of plain media was added, and the remaining cells were scraped out of the 75 cm² flask with a cell scraper and added to the 50 mL tube. Cells were centrifuged at 200×g for 5 minutes at room temperature, and the media was aspirated. The cell pellet was resuspended in 10 mL complete growth media (F12 (Life Technologies, Cat #: 31765092)+15% FBS—heat inactivated (Hyclone, Cat #: SH30071.03) H-IXPen-Strep (Life Technologies, cat #: 15410-122)). Cell number was determined using a hemacytometer. Cells were then seeded at 4000 cells per well of a 96-well plate in 100 μL of complete growth media. The plate was incubated overnight at 37° C. and 5% CO₂ in a water-jacketed incubator.

The next day, 80 μL of fresh complete media was added to each well, and the NR8383 cells were challenged with treprostinil compound treatments. Following a 72 hour incubation at 37° C and 5% CO₂ in a water-jacketed incubator, the inhibitory effect on cell proliferation was determined. Measurements and calculations were made as described above for the CHO—K1 cells.

Effect of Treprostinil Alkyl Ester Compositions on CHO—K1 Cell Proliferation

CHG-K1 cells were challenged with compositions comprising treprostinil alkyl ester derivatives:

-   T554 (C₂-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T543 (C₆-TR 40 mol %, Toco Acet 40 mol %, Chol-PEG2k 10 mol %), -   T555 (C₈-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T556 (C₁₀-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T568 (C₁₂-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), -   T623 (C₁₆-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC     10 mol %), at concentrations ranging from 0.55 μM to 125 μM.     Following a 48 hour incubation period, the inhibitory effect of the     treprostinil derivative compositions on cell proliferation was     determined.

Table 8 below summarizes the effect of the above treprostinil compositions on CHO—K 1 cell proliferations. At the highest concentration of 100 μM, only T543 (C₆-TR) and T623 (C₁₆-TR) exhibited a significant inhibitory effect on cell proliferation.

TABLE 8 Effect of Treprostinil Compositions on cell proliferation. CHO-K1 Cells NR8383 Cells Samples (<100 μM-0.78 μM) (≦100 μM-0.78 μM) T543 (C₆-TR) Detectable cell inhibition Detectable cell prolifera- only at 100 μM tion inhibition only at concentration concentration >25 uM T554 (C₂-TR) No detectable cell Detectable cell prolifera- proliferation tion inhibition at inhibition 70 μM T555 (C₈-TR) No detectable cell Detectable cell prolifera- proliferation tion inhibition only at inhibition concentration >50 μM T556 (C₁₀-TR) No detectable cell Detectable cell prolifera- proliferation tion inhibition only at inhibition concentration >50 μM T568 (C₁₂-TR) No detectable cell Detectable cell prolifera- proliferation tion inhibition only at inhibition concentration >100 μM T623 (C₁₆-TR) Detectable cell prolifera- Detectable cell prolifera- tion inhibition only at tion inhibition only at 100 μM concentration 100 μM concentration

Effect of Treprostinil Compositions on NR8383 Cell Proliferation

Rat alveolar NR8383 cells were challenged with the same treprostinil deri vative composi tions:

T543 (C₆-TR 40 mol %, Toco Ace 40 mol %, Chol-PEG2k 20 mol %), T554 (C₂-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %), T555 (C₈-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %), T556 (C₁₀-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %), T568 (C₁₂-TR 40 mol %, squalane 40 mol %, ChoI-PEG2k 10 mol %, DOPC 10 mol %), and T623 (C₁₆-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %), at the same concentrations (0.55 μM to 125 pM) as the CHO—K1 cells above. Following a 72 hour incubation period, the inhibitory effect of the treprostinil derivative compositions on cell proliferation was determined.

Table 8 above summarizes the effect of the above treprostinil compositions on NR₈₃₈₃ cell proliferation. At the highest dose of 100 μM, all of the treprostinil derivative compositions demonstrated some inhibition of cell proliferation, and T543 (C₆-TR.) exhibited the greatest inhibitory effect.

Effect of Treprostinil Alkyl Ester Compounds on Cell Proliferation

In order to determine any effect of treprostinil derivative compounds (unformulated) on cell proliferation, the cell based assays described above, using CHO—K1 cells and rat alveolar cells (NR8383 cells) were performed.

CHO-K1 Cell Proliferation Assay

CHO—K1 cells were challenged with treprostinil alkyl esters, i.e., TR compounds of Formula (A), having the following R₂ groups:

-   C₂, C₃, C₄, C₅, C₆, C₈, C₁₀ or C₁₂ straight chain alkyl, at dosages     ranging from 0.098 μM to 25 μM, Following a 48 hour incubation     period, the inhibitory effect on cell proliferation was determined.

Table 9 below summarizes the effect of the above treprostinil alkyl esters on CHO—K1 and NR8383 cell proliferation. At the highest concentration, only the treprostinil octyl ester compound showed inhibition of cell proliferation.

TABLE 9 Effect of treprostinil alkyl esters on cell proliferation CHO-K1 Cells NR8383 Cells Samples (0.195 μM-25 μM) (0.195 μM-25 μM) C₂-TR No detectable cell inhibition No detectable cell inhibition C₃- TR No detectable cell inhibition No detectable cell inhibition C₄-TR No detectable cell inhibition No detectable cell inhibition C₅- TR No detectable cell inhibition No detectable cell inhibition C₆-TR No detectable cell inhibition No detectable cell inhibition C₈-TR Detectable cell inhibition at Some detectable cell 25 μM inhibition C₁₀-TR No detectable cell inhibition No detectable cell inhibition C₁₂-TR No detectable cell inhibition No detectable cell inhibition

NR8383 Cell Proliferation Assay

Rat alveolar NR₈₃₈₃ cells were challenged with treprostinil compounds derivatized at the R₂ position of Formula (A) with a C₂, C₃, C₄, C₅, C₆, C₈, C₁₀ or C₁₂ straight chain alkyl moiety at concentrations ranging from 0.195 μM to 25 μM. Following a 72 hour incubation period, the inhibitory effect on cell proliferation was determined.

Table 11 above summarizes the effect of the above treprostinil alkyl esters on NR8383 cell proliferation. Similar to the CHO—K1 cell assay, only the treprostinil octyl ester showed some inhibition of cell proliferation at the highest concentration.

Treprostinil Derivative Compositions—Effect on Cell Proliferation

In order to determine the effect of treprostinil derivative compositions on cell proliferation, cell based assays using CHO—K1 cells and rat alveolar cells (NR8383 cells) were performed.

Effect of Treprostinil Compositions on CHO Cell Proliferation

CHO—K1. cells were challenged with treprostinil derivative compositions: T596 (C₂-TR 45 mol %, DSG-P2K 55 mol %), T597 (Q-TR 45 mol %, DSG-P2K 55 mol %), T598 (C₈-TR 45 mol %, DSG-P2K 55 mol %), T599 (C₁₀-TR 45 mol %, DSG-P2K 55 mol %), and T600 (C₁₂-TR 45 mol %, DSG-P2K 55 mol %), T612 (C₂-TR 10 mol %, DMPE-PIK 90 mol %), T613 (C₈-TR 10 mol %, DMPE-P1K 90 mol %), at concentrations ranging from 0.23 μM to 29 μM. Following a 72 hour incubation period, the inhibitory effect on cell proliferation was determined. Following a 48 hour incubation period, the inhibitory effect on cell proliferation was determined.

Table 10 below summarizes the effect of the treprostinil compositions on CHO—K1 cell proliferation. None of the compositions tested exhibited a significant inhibitory effect on CHO—K1 cell proliferation.

TABLE 10 Effect of treprostinil compositions on cell proliferation. Samples CHO-K1 Cells NR8383 Cells Sample concentration (29 μM-0.23 μM) (29 μM-0.23 μM) T596 (C₂) No detectable cell Some detectable cell prolifera- proliferation tion inhibition only at inhibition concentration >25 uM T597 (C₆) No detectable cell Some detectable cell prolifera- proliferation tion inhibition at 70 uM inhibition T598 (C₈) No detectable cell Some detectable cell prolifera- proliferation tion inhibition only at inhibition concentration >50 uM T599 (C₁₀) No detectable cell Some detectable cell prolifera- proliferation tion inhibition at ≧14.5 inhibition uM concentration T600 (C₁₂) No detectable cell Some detectable cell prolifera- proliferation tion inhibition at ≧14.5 inhibition uM concentration Sample concentration (180 μM-1.41μM) (180 μM-1.41 μM) T612 (C₂) Detectable cell prolifera- Detectable cell prolifera- tion inhibition at ≧90 tion inhibition only at 180 μM concentration μM concentration T613 (C₈) Detectable cell prolifera- Detectable cell prolifera- tion inhibition at ≧90 tion inhibition only at 180 μM concentration μM concentration

Similarly, CHG-K1 cells were challenged with the treprostinil compositions T612 (R₂═C₂), T613 (R₂═C₈) at concentrations ranging from 1.41 μM to 180 μM. After 48 hours, the inhibitory effect on cell proliferation was determined, and all four of the treprostinil compositions exhibited 100% inhibition of cell proliferation at the higher concentrations.

Effect of Treprostinil Compositions on NR8383 Cell Proliferation

Rat alveolar NR8383 cells were challenged with the same treprostinil compositions (above) as well as T596 (C₂-TR 45 mol %, DSG-P2K 55 mol %), T612 (C₂-TR 10 mol %, DMPE-P1K 90 mol %), T597 (C₆-TR 45 mol %, DSG-P2K 55 mol %), T598 (C₈-TR 45 mol %, DSG-P2K 55 mol %), T613 (C₈-TR 10 mol %, DMPE-P1K 90 mol %), T599 (C₁₀-TR 45 mol %, DSG-P2K 55 mol %), T600 (C₁₂-TR 45 mol %, DSG-P2K 55 mol %), and at the same concentrations (0.23 μM to 29 μM) as the CHO—K 1 cells above. Following a 72 hour incubation period, the inhibitory effect on cell proliferation was determined.

Table 10 above summarizes the effect of the treprostinil composition on NR8383 cell proliferation. All of the treprostinil compositions demonstrated some (≦10%) inhibition of NR8383 cell proliferation.

Example 6 Treprostinil Compounds In Vivo

The effect of treprostinil derivative compounds in vivo was determined by using rat models. Young male rats Sprague Dawley (Charles River) were used for the study. Rats anesthetized with ketamine/xylazine, placed on a heating pad and after surgical isolation and catheterization of the trachea, mechanically ventilated throughout the study.

A catheter was placed in the femoral artery for measurement of systolic (sys) and diastolic (dias) blood pressures. A thoracotomy was performed and a catheter inserted into the right ventricle and positioned in the pulmonary artery for the measurement of pulmonary arterial systolic and diastolic blood pressures. Oxygen saturation (SaO₂) was measured with a pulse oximeter placed on the paw.

With the rats ventilated on room air (FIO₂=0.21), cardiovascular measurements were made under these normoxic conditions. In order to induce hypoxia the FIO2 was reduced over a 30 min period until SaO2 fell to values between 50-60%, and a baseline hypoxia value for each of the parameters was determined.

Groups of four rats each received either PBS, free treprostinil (1.7 μg/kg and 10 μg/kg), or a composition comprising C₂-TR (T554); C₈-TR (T555: C₈-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %) (38.6 μg/kg), C₁₀-TR (T556: C₁₀-TR 40 mol %, squalane 40 mol %, Chol-PEG2k 10 mol %, DOPC 10 mol %) (40.8 μg/kg)), C₁₂-TR (T568).

The target dose varied slightly by weight due to the differences in molecular weight of the treprostinil derivative compositions as shown in Table 11 below. The actual achieved lung dose was about 5× lower than provided in Table 11 (e.g., administration of 10 μg/kg ylelded about 2 μg/kg in the lungs). The various treatments were delivered (via inhalation of nebulized drug to the lungs of the rats. The pulmonary arterial pressure (PAP), systemic arterial pressure (SAP), and heart rate of the rats were measured continuously for 180 minutes. The PAP signal was collected at 200 points per second.

TABLE 11 Target Doses in Acute Hypoxia Rat Model Target Dose Target Dose (μg/kg) (nmole/kg) Treprostinil 1.7 4.35 10 25.6 30 76.8 Treporostinil C₂* 32.1 76.8 derivative C₆* 36.4 76.8 compound C₈* 38.6 76.8 C₁₀* 40.8 76.8 C₁₂* 42.9 76.8 C₁₆* 47.2 76.8 *Indicates alkyl chain length at position R₂ of the compound of Formula (A).

The normalized variation of mean PAP (mPAP) is shown as a percentage from the hypoxic baseline value at (T=0) in FIG. 15. The hypoxic baseline PAP value was 100%, and the changes in pressure were measured in comparison to the hypoxic baseline. The normalized variation of mean SAP (mSAP) is shown as a percentage from the hypoxic baseline value in FIG. 16. Heart rate is shown in FIG. 17 as a percentage of the hypoxic baseline value over time.

Example 7 Measurement of Cyclic Adenosine Monophosphate (cAMP) Levels in CHO—K1 Cells in Response to 5-nonanyl-TR

A cell based Chinese hamster ovary-K1 (CHO—KT) assay based on the GloSensor™ cAMP assay (Promega) was used as described above in Example 4 to characterize the effect of the following compounds on cAMP levels:

-   -   5-nonanyl-TR, i.e., the compound of Formula (A) wherein         R₂=5-nonanyl

-   -   C₁₂-TR i.e., i.e., the compound of Formula (A) wherein R₂═C₁₂         alkyl

-   -   C₁₄-TR, i.e., the compound of Formula (A) wherein R₂═C₁₄ alkyl

-   -   C₁₆-TR, i.e., the compound of Formula (A) wherein R₂═C₁₆ alkyl

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with 5-nonanyl-treprostinil (branched chain, 5C9-TR) or treprostinil alkyl ester compounds having either a C₁₂, C₁₄ or C₁₆ straight chain alkyl group at the R₂ position of the above compound. cAMP levels were then measured every 5 minutes over a time course of 8 hours. Dose response curves at 0.5 hr, 1 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr, and 8 hr incubation time for 5-nonanyl-TR, C₁₄-TR, and C₁₆-TR are provided in FIGS. 18, 19, and 20 respectively. Like C₁₄-TR and C₁₆-TR, the potency of 5-nonanyl-TR increases with incubation time, indicating a delay-release profile. The half maximal effective concentrations (EC₅₀) of the treprostinil compounds were determined using the results from the cAMP assays. EC₅₀ for 5-Nonanyl-TR, C₁₄-TR, and C₁₆-TR are shown in FIGS. 18, 19, and 20, respectively.

Kinetic profile results from the 10 μM (top panel) and 5 μM (bottom panel) concentrations of C₁₂-TR, C₁₄-TR, C₁₆-TR, or 5-nonanyl-TR are provided at FIG. 21. cAMP levels in response to C₁₂-TR, C₁₄-TR, and 5-nonanyl-TR at both concentrations increased over the first 1-1.5 hours and were sustained for at least 8 hours. The ranking of activity of the treprostinil compounds was C₁₂-TR>C₁₄-TR>5-nonanyl-TR>C₁₆-TR.

The results of the study showed that like the treprostinil alkyl ester compounds having a C₁₂, C₁₄ or C₁₆ straight chain alkyl ester group, 5-nonanyl-TR, is functional and exhibits sustained cAMP activity. Thus, unlike free treprostinil (see Example 4), 5-nonanyl-TR has a delayed release profile.

Example 8 Comparison of Cyclic Adenosine Monophosphate (cAMP) Activation in CHO—K1 Cells in Response to C₁₄-TR Formulations

A cell based Chinese hamster ovary-K1 (CHO—KT) assay based on the GloSensor™ cAMP assay (Promega) was used as described above in Example 4 to characterize the effect of different C₁₄-TR formulations on cAMP levels. The C₁₄-TR formulations are shown below in Table 12. Composition T679 does not comprise DOPC; composition T647 does not comprise DOPC or squalane.

The structure of C₁₄-TR is as follows:

TABLE 12 Components of C14-TR formulations Hydrophobic PEGylated Cx-TR Additive lipid DOPC Composition (mol %) (mol %) (mol %) mol % T631 C₁₄-TR Squalane Chol- 10% (40%) (40%) PEG2k (10%) T679 C₁₄-TR Squalane Chol- 0 (45%) (45%) PEG2k (10%) T647 C₁₄-TR (none) Chol- 0 (90%) PEG2k (10%)

CHO—K 1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with treprostinil alkyl ester formulations having a C₁₄ straight chain alkyl ester group at the carboxylic acid position and having the components as indicated in Table 12. cAMP levels were then measured every 5 minutes over a time course of 8 hours.

A dose response curve at 0.5 hr, 1 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr, and 8 hr incubation time for compound T679 is provided in FIG. 22. The potency of T679 increases over the incubation time, indicating a delay-release profile. The half maximal effective concentration (EC₅₀) of T679 was determined using the results from the cAMP assays, and is also shown in FIG. 22.

Kinetic profile comparisons for free treprostinil, T631, and T679 at 10 μM (top panel) and 5μM (bottom panel) are shown in FIG. 23. Both T631 and T679 were less potent compared to free treprostinil. However, unlike free treprostinil, cAMP activation increased over time in response to both T631 and T679 and was sustained for at least 8 hours. The results of the study showed that the T679 formulation, which is a C₁₄-TR without DOPC, is functional and exhibits a delayed release profile similar to the profile of the C₁₄-TR T631.

A dose response curve at 0.5 hr, 1 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr, and 8 hr incubation time for compound T647 is provided in FIG. 24. Like T679, the potency of T647 increases over the incubation time, indicating a delay-release profile. The half maximal effective concentration (EC₅₀) of T647 was determined using the results from the cAMP assay, and is also shown in FIG. 24.

Kinetic profile comparisons for free treprostinil, T631, and T647 at 10 μM (top panel) and 5 μM (bottom panel) are shown in FIG. 25, Both T631 and T647 were less potent compared to free treprostinil. However, unlike free treprostinil, cAMP activation increased over time in response to both T631 and T647 and was sustained for at least 8 hours. The results of the study showed that the T647 formulation, which is a C₁₄-TR without DOPC or squalane, is functional and exhibits a delayed release profile similar to the profile of the C₁₄-TR T631.

Example 9 Functional cAMP Studies for Treprostinil Alkyl Ester Nanoparticle Formulations

A cell based Chinese hamster ovary-K1 (CHO—K1) assay based on the GloSensor™ cAMP assay (Promega) was used as described above in Example 4 to characterize the effect of treprostinil compositions on cAMP levels. The cAMP profiles of the following treprostinil compositions were tested in this study (see also Table 13):

-   -   T555: C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   T556: C₁₀-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   T568: C₁₂-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   T631: C₁₄-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   T623: C₁₆-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   T637: C₁₈-TR (i.e., the compound of Formula (A) wherein R₂=

TABLE 13 Treprostinil Alkyl ester formulations used in Example 9. Formula- Treprostinil Treprostinil Chol- tion alkyl ester alkyl ester Squalane DOPC PEG2k No. (Cx-TR*) (mol %) (mol %) (mol %) (mol %) T555 C₈-TR 40 40 10 10 T556 C₁₀-TR 40 40 10 10 T568 C₁₂-TR 40 40 10 10 T631 C₁₄-TR 40 40 10 10 T623 C₁₆-TR 40 40 10 10 T637 C₁₈-TR 40 40 10 10 *Cx indicates alkyl chain length at position R₂ of the compound of Formula (A).

CHO—K1 cells co-transfected with the EP2 receptor and GloSensor™ plasmid were challenged with the treprostinil alkyl ester compositions listed above. cAMP levels were then measured every 5 minutes over a time course of 8 hours.

A dose response curve at 0.5 hr, 1 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr, and 8 hr incubation time for composition T637 (C₁₈-TR) is provided in FIG. 26. The potency of T679 increases over the initial incubation time and then remains at a sustained level for at least 8 hours, indicating a delay-release profile. The half maximal effective concentration (EC₅₀) of T637 was determined using the results from the cAMP assays, and is also shown in FIG. 26.

Kinetic profile comparisons for free treprostinil, T555, T556, T568, T631, T623, and T637 at 10 μM (top panel) and 5 μM (bottom panel) are shown in FIG. 27. Each of the treprostinil alkyl ester compounds were less potent compared to free treprostinil. However, unlike free treprostinil, cAMP activation increased and then remained at a sustained level for at least 8 hours in response to each of the treprostinil alkyl ester compounds, indicating that each of these compounds is functional and exhibits a delayed release profile. The ranking order of activity for these compounds was T555/T556>T568>T631>T623>T637.

Example 10 Enzymatic Conversion Kinetics of Branched Treprostinil Compounds

A set of studies was conducted to determine the conversion kinetics to treprostinil of linear treprostinil compounds versus various branched treprostinil compounds. 0.4 mM of linear C₈-TR or branched treprostinil compounds 2-dimethyl-1-propanyl-TR, 3,3-dimethyl-1-butanyl-TR, 2-ethyl-1-butanyl-TR, 5-nonanyl-TR, or 3-pentanyl-TR (see below for structures) were incubated with 0.2 U esterase at 37° C. for 1 hour, and the conversion (% of total) was calculated at 0.25, 0.5, 0.75, or 1 hour incubation time.

-   -   C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   2-dimethyl-1-propanyl-TR (i.e., the compound of Formula (A)         wherein R₂=

-   -   3.3-dimethvl-1-hutanvl-TR (i.e.. the compound of Formula (A)         wherein R₂=

-   -   2-ethyl-1-butanyl-TR (i.e., the compound of Formula (A) wherein         R₂=

-   -   5-nonanyl-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   3-pentanyl-TR (i.e., the compound of Formula (A) wherein R₂=

FIG. 28 shows that 5-nonanyl-TR exhibited a slower conversion rate than linear C8-TR.

FIG. 29 shows the esterase mediated conversion of the following treprostinil compounds to treprostinil: C₈-TR, C₉-TR, C₁₀-TR, C₁₂-TR, C₁₄-TR and C₁₆-TR, i.e., where R₂ is as follows for the following formula. The conversion is relative to the C₈-TR compound and conversion was measured at 1 hr. post esterase incubation,

-   -   C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   C₉-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   C₁₀-TR (i.e.. the compound of Formula (A) wherein R₂=

-   -   C₁₂-TR (i.e.. the compound of Formula (A) wherein R₂=

-   -   C₁₄-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   C₁₆-TR (i.e., the compound of Formula (A) wherein R₂=

FIG. 30 shows the esterase mediated conversion of branched treprostinil compounds (below) to treprostinil relative to esterase mediated conversion of C₈-TR to treprostinil. Conversion was measured at 1 hr. post esterase incubation.

-   -   4C₇-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   4C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   3C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   2C₈-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   5C₉-TR (i.e., the compound of Formula (A) wherein R₂=

-   -   2C₉-TR (i.e., the compound of Formula (A) wherein R₂=

Each of the branched compounds 4C7-TR, 4C8-TR, and 5C9-TR exhibited a slower conversion rate than the linear compound C₈-TR. The asymmetrical branched compound (4C₈-TR) exhibited a slower conversion rate than the symmetrical compounds (4C₇-TR and 5C₉-TR). Further, there was no significant difference between the conversion rates of R and S isomers of 2C₈-TR ((R)-2C₈-TR versus (S)-2C₈-TR).

Example 11 Measurement of Treprostinil Pharmacokinetics in Rats

Table 14 provides the treprostinil alkyl ester formulations used in this study. The first three compositions (T568, T631 and T623) are believed to form lipid nanoparticl.es, while the last three compositions (T630, T635 and T636) are believed to form micelles.

TABLE 14 Alkyl ester formulations used in Example 11. Treprostinil DMPE- Formulation Treprostinil alkyl ester Squalane DOPC (mol Chol-PEG2k Peg2k (mol No. alkyl ester (mol %) (mol %) %) (mol %) %) T568 C₁₂-TR 40 40 10 10 — T631 C₁₄-TR 40 40 10 10 — T623 C₁₆-TR 40 40 10 10 — T630 C₁₂-TR 10 — — — 90 T635 C₁₄-TR  5 — — — 95 T636 C₁₆-TR  5 — — — 95

Nebulized treprostinil (TRE) solution and treprostinil alkyl ester formulations were administered (at 15 nmol/kg, or 6 mg/kg TRE equivalent) to anaesthetised-ventilated rats (6-hour studies) or to conscious rats by nose-only inhalation (24-hour studies). Blood and lung samples were collected at specified time points. TRE and treprostinil alkyl ester concentrations in blood plasma and lung tissue were measured by HPLC/MS/MS analysis.

Anaesthetized, Venitlated Rats

Male Sprague Dawley rats wrere anaesthetised and prepared with endotracheal tube for ventilation. The right femoral vein was cannulated to facilitate blood collections. Terminal lung samples were taken for analysis only 6 hours after dosing. Aeroneb® nebulizer and a controller (Aerogen, Galway, Ireland) were used to produce aerosol of a mass median aerodynamic diameter (MMAD) between 2.5 μm and 4 μm and at a rate of 0.1 mL/min to provide an estimated pulmonary dose of 6 μg/kg. A SAR-830/AP Small Animal Ventilator (CWE Inc., Ardmore, Pa.) set up at ventilator tidal volume (VT) of 8 mL/kg, rate of 90 breaths/min, was used to deliver nebulized test articles of volume 250 μL. Systemic blood pressure (mSAP), heart rate (HR), and arterial oxygen saturation (SaO2). Physiologic parameters were measured during normoxia (fraction of inspired oxygen [FrO₂]=0.21, SaO₂ ≈90%) and for 2 to 3 hours during hypoxia (FrO₂=0.10, SaO₂≈50%).

Conscious Nose-Only Inhalation

Male Sprague Dawley rats were placed in restraining tubes and exposed to nebulised drugs via the Jaeger-NYU Nose-Only Directed-Flow Inhalation Exposure System (CH Technologies, Westwood, N.J.) (FIG. 31), Test articles (6 mL at specific concentration) were nebulised using the Aeroneb nebuliser to deliver a predetermined estimated pulmonary dose. Blood and lung tissue samples were taken at selected times after nebulization of the drags over a 24-hour period.

Ventilated rats treated with nebulized TRE solution had the highest blood plasma concentration (Cmax) (3.5 ng/mL), which occurred immediately after dosing (FIG. 32, left). Measurable levels of TRE were not seen beyond 4 hours in the blood plasma and by 6 hours in the lungs. In contrast, ventilated rats treated with nebulized TPD-LNP had lower blood plasma TRE Cmax values, ranging from 0.2 ng/mL to 0.6 ng/mL (Table 15, FIG. 32, left). At 6 hours, treprostinil alkyl ester remained in the lung at levels that ranged from 100 ng/g to 400 ng/g tissue of TRE equivalent (FIG. 33). Treprostinil detected in the lung was speculated to be generated due to treprostinil alkyl ester hydrolysis during sample preparation. When dosing with micellar TPD, blood plasma levels of TRE were higher than with TPD lipid nanoparticle formulations, indicating that nanoparticles play an additional role in slow-release effect (FIG. 32, comparison of left and right graphs). In the 24-hour studies in rats dosed with TPD-lipid nanoparticle formulations (nose-only inhalation), TRE Cmax was higher than in ventilated animals and showed close to first-order exponential decline. Blood plasma concentrations of TRE in rats that received dosing with C₁₄- and C₁₆-treprostinil alkyl ester lipid nanoparticle formulations wrere maintained at greater than 0.1 ng/mL for up to 24 hours, (levels corresponding to activity in acute hypoxia studies) (FIG. 34, top). Lung levels of total TRE+TPD were approximately 103 higher than plasma TRE and also exhibited exponential decline in rats administered treprostinil alkyl ester lipid nanoparticle formulations (FIG. 34, bottom). Table 16 further shows the pharmacokinetics of treprostinil in rats after dosing with the nose-only stystem with the nebulized treprostinil alkyl ester lipid nanoparticle formulations at the estimated pulmonary dose of 6 μg/kg. FIG. 35 further shows that release kinetics of treprostinil from inhaled C₁₆-TR formulations over 24 hours is independent of dose (nose only dosing). Time in FIG. 35 corresponds to the time after beginning of nebulization of a 6 mL suspension (nebulization period was 30 min, to 60 min.). FIG. 38 shows that animals treated with T568 and T623 had a survival benefit (surviving beyond 200 minutes) compared with animals treated with free treprostinil or PBS). Specifically, FIG. 38 shows the pulmonary arterial pressure in animals treated with various lipid nanoparticle formulations, PBS and treprostinil. Furthermore, treatment with T568 and T623 showed little impact on systemic haemodynamics (FIG. 39). Finally, treprostinil alkyl ester nanoparticle formulations were shown to convert sloly to treprostinil, providing consistent blood plasma levels with reduced peak values (FIG. 40).

TABLE 15 Plasma pharmacokinetics of treprostinil in ventilated rats after dosing with nebulized treprostinil solution or formulated treprostinil alkyl ester suspension at an estimated pulmonary dose of 6 μg/kg Lipid Nanoparticles Micelles (T568, T631 and T623) (T630, T635 and T636) Solution T568 T631 T623 T630 T635 T636 (C_(x)-TR) (C₁₂-TR) (C₁₄-TR) (C₁₆-TR) (C₁₂-TR) (C₁₄-TR) (C₁₆-TR) AUC 0-6 h 2.13 4.47 3.89 1.84 9.72 9.11 5.35 (ng * h/mL) Cmax 3.37 0.56 0.34 0.22 2.40 1.20 0.84 (ng/mL) Tmax (h) 0.05 0.5 0.5 1.0 0.05 0.5 1.0

TABLE 16 Pharmacokinetics of treprostinil in rats after dosing with the nose- only stystem with the nebulized treprostinil alkyl ester formulations (T568, T631 and T623) at the estimated pulmonary dose of 6 μg/kg Compound C₁₂-TR C₁₄-TR C₁₆-TR immediately post dose (IPD) (μg/kg) 6.2 10.4 17.9 Lung apparent ellimination rate (h⁻¹) 0.42 0.15 0.10 Plasma maximum concentration (Cmax) IPD 4.03 4.93 3.46 (ng/mL) Plasma apparent elimination rate (h⁻¹) 0.30 0.18 0.14 Area Under Curve (AUC) 1-24 (ng*h/mL) 11.9 24.0 17.9

Inhaled TPDs are present in the lungs for an extended duration and are associated with a slow, sustained release of TRE into the blood. This duration of activity is increased with TPD formulated in lipid nanoparticles.

Example 12 Pharmacokinetic Profile of C₁₆-TR Alkyl Ester Lipid Nasioparticle Formulation in Dogs

Twelve beagle dogs of either sex were randomly assigned to different inhaled doses of treprostinil in PBS or the compound of Formula (A) wherein R₂=

(C₁₆-TR) formulated in a lipid nanoparticle formulation (T623) that is suspended in PBS (see Table 14), with both given by nebulizer. Formulations were nebulized with an Aeroneb nebulizer (MMAD: 2.5-4 μm) delivered into a 500 ml expansion chamber. Formulations were nebulized for 2 min at ventilator settings of 90 ml/breath, 15 breaths/min (delivered volume=2.7 L) and collected on a filter. Drug amount (μg) on the filter was measured by HPLC to calculate the concentration of drug delivered through the ventilator circuit (μg/L).

Dosimetry was performed in propofol-anesthetized dogs in which nebulized drugs were introduced into a mixing chamber interposed on the inspiratory limb of a canine respirator. Technical trials were performed before each experiment to measure the concentration of drug (μg/L) delivered for each breath. The inhaled drug dose (μg/kg) was calculated using the formula: Inhaled Drug Dose (μg/kg)=Drug Cone. (μg/L)×Minute Ventilation (L/min.)×Time (min.)/Body Weight (kg). After delivery of the drugs, the dogs were disconnected from the respirator and blood samples were collected over a 72 h period to measure the treprostinil plasma concentrations by HPLC/MS/MS, Clinical signs were monitored over this 72 hr. period,

Use of the anesthetized, intubated and ventilated approach provided reproducibility between dogs to achieve the targeted inhaled dose for both treprostinil (5 I and 16±2 μg kg) and C₁₆-TR (7±1, 22±1, 46±1 and 95±1 μg kg). At inhaled doses of 5 and 16 μg/kg, treprostinil plasma Cmax values for dogs dosed with treprostinil (2.7 and 5.9 ng/ml, respectively) were between 15-20 fold higher compared to treprostinil levels achieved upon dosing with similar inhaled doses (7 and 22 μg/kg) of C₁₆-TR in the T623 formulation (0,2 and 0.3 ng/mL, respectively) (FIG. 36). Furthermore, the plasma levels of treprostinil were sustained over a 48 hour period with inhalation of T623 but disappeared within a few hours following inhalation of treprostinil (FIG. 36). Coughing and rapid shallow breathing were absent during delivery of treprostinil to anesthetized, ventilated dogs but were present during the recovery period. Dogs receiving T623 showed no signs of respiratory irritation with inhaled doses as high as 46 μg/kg.

Comparison of C₁₆ Alkyl Ester Lipid Nanopartide Treprostinil Formulation to C₁₂ and C₁₄ Alkyl Ester Lipid Nanoparticle Treprostinil Formulations

Twelve beagle dogs were exposed to inhaled treprostinil and three treprostinil alkyl ester lipid nanoparticle formulations: T568 (dodecyl-treprostinil, C₁₂-TR), T631(tetradecyl-treprostinil, C₁₄-TR) and T623 (hexadecyl-treprostinil, C₁₆-TR). The components of each formulation are provided in Table 14, above.

Dosimetry was performed in propofol-anesthetized, artificially ventilated dogs in which nebulized drugs were introduced into a mixing chamber interposed on the inspiratory limb of the respirator. Technical trials were performed before each experiment measuring the concentration of drug (μg/L) per breath, minute ventilation and time required to achieve a targeted pulmonary dose. After recovery from the anesthesia, blood samples were collected over 72 h and plasma levels of TRE measured by BPLC/MS/MS. Clinical signs (cough, rapid shallow breathing, emesis and pale gums) were also monitored.

At a targeted pulmonary dose of 18 μg/kg, plasma levels of treprostinil were highest for free treprostinil (Cmax=5.9±0.6 ng/ml) immediately after dosing but corresponding Cmax values for C₁₂-TR, C₁₄-TR and C₁₆-TR were 5-, 13- and 20-fold lower. Plasma treprostinil was below the level of quantification by 4 h after inhaled free treprostinil, but was sustained for 48-72 h after inhaled treprostinil alkyl ester formulations.

Dose-dependent increases in Cmax and AUG were seen with inhaled C₁₆-TR (6-90 μg/kg) with a prolonged presence of treprostinil in the plasma for up to 72 h at higher doses. Adverse clinical signs were seen with free treprostinil and C₁₂-TR at a targeted dose of 18 μg/kg, but not with C₁₄-TR and C₁₆-TR. In the dose-response study with C₁₆-TR, adverse clinical signs were seen in only 1 dog at a targeted pulmonary dose of 90 μg/kg,

Based upon this PK study in dogs, inhaled C₁₆-TR in a nanoparticle formulation provides sustained presence of treprostinil in the plasma and lower side effect potential than inhaled free treprostinil at comparable doses.

Example 13 Characterization of a Lipid Nanoparticle C₁₆ Alkyl Ester Treprostinil Formulation

T748, a lipid nanoparticle C₁₆ alkyl ester treprostinil formulation having the following components, was characterized.

C₁₆-TR Squalane DSPE-PEG2k (mol %) (mol %) (mol %) 45 45 10

Assessment of the Tolerability and Pharmacokinetics (PK) of Treprostinil in Rats administerd T748 lipid nanoparticle formulation

To assess whether repeated dosing with inhaled C₁₆-TR is well tolerated and alters PK, rats were exposed to C₁₆-TR for 14-consecutive days.

5 groups (n=4 per group) of Sprague Dawley rats were exposed to inhaled phosphate buffered saline (PBS) or 4 doses of C₁₆-TR (0.6, 1.8, 6 and 18 μg/kg) given by nebulization in a nose-only inhalation chamber. Cohorts of rats were studied after 1, 7 and 14 daily inhaled doses of C₁₆-TR and blood samples were collected at 1, 3, 6 and 24 hr,, and lungs harvested at 24 hr. after the last dose of the drug. Concentrations of treprostinil and C₁₆-TR. in the plasma and lungs were measured by HPLC/MS/MS. Body weights were recorded daily and organ weights (lungs, heart, liver) were measured 24 hr, after the last drug dose.

There were no tolerability issues or significant changes (relative to PBS) in body weights and organ weights after inhalation of C₁₆-TR for 14-conseeutive days. Increasing inhaled doses of C₁₆-TR (0.6-18 μg/kg) increased the plasma Cmax and AUC but this was not consistently affected upon repeated dosing. There was some variability in AUC between days 1 and 14 within the different dosing groups with 2 of the 4 doses (1.8 and 18 μg/kg) showing no difference, and the other 2 doses (0.6 and 6 μg/kg) showing a 3- to 4-fold increase in AUC by day 14. The presence of C₁₆-TR was not detected in the plasma at any dose. However, relatively high concentrations of C₁₆-TR (approximately 1,000-fold higher than plasma treprostinil) were found in the lungs. Inhaled C₁₆-TR produced a dose-dependent increase in the concentration of C₁₆-TR. in the lungs, but this was not changed by repeated dosing for 14-consecutive days.

Inhaled C₁₆-TR (0.6-18 μg/kg) was well tolerated with no evidence of body weight and organ weight change after dosing for 14 consecutive days.

Effect of C₁₆ Alkyl Ester Lipid Nanoparticle Treprostinil Formulation on the Cough Reflex in Guinea Pigs

In this study, the tussive effects of inhaled treprostinil and a lipid nanoparticle formulation of the alkyl ester hexadecyl-treprostinil (C₁₆-TR), were studied in guinea pigs.

Three groups of male Dunkin Hartley guinea pigs were placed in a whole body plethysmograph and exposed to aerosolized phosphate buffered saline (PBS), TRE (1-300 μg/ml) and C₁₆-TR lipid nanoparticle formulation T748 (30 μg/ml), respectively. T623 has the following components:

Aerosols were generated with an Ultra-Neb Pro nebulizer (nebulizer output 0.36 mL/min.) that was mixed with inspired air delivered at a rate of 2 L/min. The PBS or drugs were delivered for 10 min. and the number of coughs recorded during and for 20 min. after the delivery. Coughs were detected by visual observations, plethysmograph recordings and cough sounds.

Exposure to aerosolized PBS did not induce cough. TRE exposure did not consistently evoke cough in the animals tested until the exposure concentration was equal to or greater than 30 μg/mL. The cough response was characterized by bouts of high frequency cough with lowered cough sounds compared to the typical cough sound induced by citric acid or capsaicin. TRE at a nebulized concentration of 30 μg/mL produced consistent cough in 7 of 7 guinea pigs with 1-4 cough bouts and a total number of coughs averaging 36+9 coughs. In contrast, inhaled C₁₆-TR lipid nanoparticle formulation at a nebulized concentration of 30 μg/mL did not induce cough, no events, in 6 of 6 guinea pigs.

The results in this study demonstrate that inhaled TRE induces cough in guinea pigs, the profile of which is somewhat similar to that previously described (Type II coughs) with inhaled prostaglandins in guinea, pigs (Maher and Belvisi, 2010). On the other hand, inhaled C₁₆-TR lipid nanoparticle formulation, did not. induce cough and suggests that this formulation may eliminate some of the local adverse side effects such as cough seen with inhaled TRE therapy in humans.

Example 14 Acylation of Treprostinil Derivatives

Treprostinil or treprostinil ester derivatives (e.g., derivatized with alkyl or alkenyl groups at the carboxylic acid moiety as prepared in Example 1) are acylated as follows.

The compound of Example 1 (0.05 mol) or treprostinil is dissolved in 10 mL of dichloromethane at 0 ° C. Dimethylaminopyridine is added (20 mol %), and then a solution of an acyl chloride R(CO)Cl (2.1 equivalents) at 0° C. (wherein R is R₅ or R₆ as described herein) is added to the compound of Example 1 or treprostinil. The solution is allowed to stir and warm to 23° C. over 1 hour. The reaction is monitored by thin layer chromatography, and when no further change is observed, the reaction is quenched with NaHCO₃ (sat), and the quenched mixture is extracted with dichloromethane (3×10 mL). The combined organic extracts are dried over anhydrous sodium sulfate, and the solvent is removed under vacuum to afford the crude product. Purification is effected by column chromatography on silica gel with 2% methanol in dichloromethane.

A general scheme for synthesis of the acylated treprostinil-derivatives is shown below (R₂ is described herein, for example as H or a linear or branched alkyl group):

Other acylation techniques known in the art, including selective acylation of each of the secondary alcohols, can be employed. In addition, R₂ can be selected such that the R₂ group can be selectively removed from the compound of Example 11 after acylation of the secondary hydroxyl functionalities. Such protecting group strategies are well known to those skilled in the art, and are described in, e.g., Peter G. M, Wutes and Theodora W. Greene, Greene's Protective Groups in Organic Synthesis, 4th Edition, Wiley (2006), which is incorporated herein by reference in its entirety for all purposes. An exemplary scheme of such a process is shown below:

Synthesis of C₁₆TR-OAc:

To a solution of (1R,2R,3aS,9aS)-[[2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3S)-3-hydroxyoctyl]-1H-benz[f]inden-5-yl]oxy]acetic acid (treprostinil) (78.1 mg, 200 μmoles) dissolved in 1,4-Dioxane (2.0 mL) was added triethylamine (TEA) (98 μL, 700 μmoles, 3.5 equivalents), acetic anhydride (166 μL, 1,760 μmoles, 8.8 equivalents), and a catalytic amount of dimethylaminopyridine (DMAP). The reaction mixture was allowed to shake at 40° C for 72 hours. Solvent was removed under reduced pressure to yleld a thick colorless oil. The crude material was dissolved in hexan.es and washed with a solution of saturated NaHCO₃ (3×5 mL). The organic layers were combined and solvent was removed using a gentle stream of wanned N₂ gas and gentle heat to yleld a thick colorless oil. The crude material was dissolved in 20% ^(n)PrOH/Hexanes, passed through a 0.45 μm syringe filter, and submitted to preparatory HPI.C purification. Solvent was removed from the purified material using a gentle stream of warmed N₂ gas and gentle heat to yleld a thick colorless oil. The pure material was suspended in ethyl lactate for storage and was submitted to analytical HPLC for concentration determination.

C₁₆-TR-QAc: 73% overall yleld. The compound was also characterized by NMR spectroscopy:

¹H NMR (500 MHz, CDCl₃) δ 0.89 (t, J=7.0 Hz, 6H), 1.17-1.32 (m, 33H). 1.43-1.46 (m, 2H), 1.49-1.66 (m, 8H), 1.89-1.93 (m, 1H), 1.99 (s, 3H), 2.06 (s, 3H), 2.30-2.35 (m, 2 h), 2.47 (d of d, J=14.5 Hz, J=6.0 Hz, 1H), 2.55 (d of d, J=15.0 Hz, J =6.0 Hz, 1H), 2.76 (d, of d, J=14.5 Hz, J=6.0 Hz, 1H). 2.90 (d of d, J=15.0 Hz, J=6.0 Hz, 1H), 4.19 (t, J=7.0 Hz, 2H), 4.62 (s, 2H), 4.70-4.74 (m, 1H). 4.87 (p, J=6.0 Hz, 1H). 6.63 (d, J=8.0 Hz, 1H), 6.82 (d, J=8.0 Hz, 1H). 7.08 (t, J=8.0 Hz, 1H) ppm; ¹³C NMR (125 MHz, CDCl₃) δ 14.2, 14.3, 21.5 (2), 22.7, 22,9, 25.1, 26.0 (2), 28.3, 28.8, 29.4, 29.6, 29,7, 29.8, 29.9, 31.9, 32.1, 33.6, 33,7, 34.3, 37.8, 40.7, 49.0, 65,6, 66.2, 74.6, 79.0, 109,8, 121.8, 126.4, 127.6, 140.7, 155.1, 169.6, 171.0, 171.1 ppm.

Example 15 Synthesis of Treprostinil Amide Derivatives

Treprostinil is available commercially, and can be synthesized, for example, by the methods disclosed in U.S. Pat. Nos. 6,765,117 and 8,497,393. Synthesis of prostaglandin derivatives is described in U.S. Pat. No. 4,668,814. The disclosures of U.S. Pat. Nos. 6,765,117; 8,497,393 and 4,668,814 are each incorporated by reference in their entireties for all purposes.

To a solution of (1R,2R,3aS,9aS)-[[2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3S)-3-hydroxyoctyl]-1H-benz[f]inden-5-yl]oxy]acetic acid (i.e., treprostinil) (78.1 mg, 200 μmoles) dissolved in 1,4-Dioxane (2.0 mL) was added triethylamine (TEA) (98 μL, 700 μmoles, 3.5 equivalents), alkylamine R₁—NH (240 μmoles, 1.2 equivalents), and a solution of PyBOP (364 mg, 700 μmoles, 3.5 equivalents) dissolved in 2.0 mL MeCN (acetonitrile).

The reaction mixture was heated to 40° C. and allowed to shake at approximately 100 rpm overnight. Solvent was removed under reduced pressure to yleld the crude product as a thick yellow oil. The product was extracted (1-1 extraction) from the oil by repeated washings with 20% BPrOH/Hexanes (3×3 mL). Solvent was removed from the organic extract using a gentle stream of warmed N₂ gas and gentle heat to yleld a thick, slightly yellow oil. The crude material was dissolved in 20% ^(n)PrOH/Hexanes, passed through a 0.45 μm syringe filter, and submitted to preparatory HPLC purification. Solvent was removed from the purified material using a gentle stream of warmed N₂ gas and gentle heat to yleld a thick, colorless oil. The pure material was suspended in ethyl lactate for storage and was submitted to analytical HPLC for concentration determination.

The following treprostinil amide derivatives of Formula B were made by the synthesis scheme provided above. (Table 17) Percentage yleld is also provided in parentheses.

TABLE 17 Treprostinil amide derivatives Compound R₁ group Yield abbreviation

88% C₁₆-TR-A

71% C₁₄-TR-A

57% C₁₂-TR-A

62% C₁₀-TR-A

47% C₈-TR-A

72% ^(t)C₈-TR-A

50% C₆-TR-A

62% ^(c)C₇-TR-A

65% 4C₇-TR-A

58% C₆-TR-A

77% C₅-TR-A

28% C₄-TR-A

12% C₃-TR-A

12% C₂-TR-A

60% Phe-EE-TR-A

Not determined Ala-EE-TR-A

Not determined Gly-EE-TR-A

Not determined Leu-EE-TR-A

C₆-TR-A and C₁₂-TR-A were characterized by NMR spectroscopy. NMR Characterization of C6-TR-A

¹H NMR (500 MHz, CDCl₃) δ 0.90 (q, J=7.0 Hz, 6H), 1.17 (q, J=12.0 Hz, 1H), 1.30-1.70 (m, 18H), 1.81-1.83 (m, 1H), 1.80-1.93 (m, 1H), 2.20 (p, J=6.0 Hz, 1H), 2.22-2.23 (m, 1H), 2.47-2.54 (m, 2H), 2.75-2.82 (m, 2H), 3.16 (sextet, J=4.0 Hz, 1H), 3.35 (q, J=7.0 Hz, 2H), 3.63 (s, 1H), 3.70-3.80 (m, 1H), 4.48 (s, 2H), 6.55 (s, 1H), 6.70 (d, J=7.5 Hz, 1H), 6.85 (d, J=7.5 Hz, 1H), 7.11 (t, J=7.5 Hz, 1H) ppm; ¹³C NMR (125 MHz, CDCl₃) δ 14.2, 14.3, 22,8, 22.9, 25.6, 26.4, 26.7(2), 28.8, 29.7, 31.6, 32.1, 33.0, 33.8, 35.1, 37.7, 39.2, 41.4, 41.6, 46.5, 52.4, 68.4, 72,8, 110.4, 122.2, 126.8, 127.3, 141.2, 154.5, 168.7 ppm; HRMS (ESI, 2:2:1 MeCN, MeOH, H₂O): m/z=474.35717 ([M+H]⁺).

NMR Characterization of C12-TR-A

HRMS (ESI, 2:2:1 MeCN, MeOH, H₂O): m/z=558.45099 ([M+H]⁺).

Example 16 Treprostinil Amide Derivative Solubility in Hydrofluoroalkane Propellants

Selected treprostinil derivatives were evaluated for the use in a metered dose inhaler (MDI). Four ester derivatives, dodecyl-treprostinil (C₁₂-TR), tetradecyl-treprostinil (C₁₄-TR), hexadecyl-treprostinil (C₁₆-TR), and the branched chain nonanyl-treprostinil (5C9-TR), and two amide derivatives, C₁₆-TR-A and C₁₂-TR-A (see Table 17) were tested for solubility in hydrofluoroalkane propellants HFA-134a and HFA-227 with added ethanol,

5 mg of each treprostinil compound was added in a glass bottle. Specific amount of ethanol was added by weight. An MDI valve was crimped to each bottle, and HFA propellant added through the valve to the total volume of 5 mL. Compounds were allowed to dissolve for 24 hours at room temperature. The formulations were assessed visually for solubility. The goal was to estimate the minimum ethanol concentration required to solubilize each compound in propellant.

Soluble samples presented as clear and colorless solutions. Less than soluble samples had a thin liquid-vapor ring of various density visible on the bottle surface at the liquid-vapor interface. Non-soluble samples had white precipitate or crystals formed. Ethanol was added as a solubility aid. As it can be seen from the solubility tables below (Table 18 and Table 19), compounds that were not soluble at 3% added ethanol became soluble at 10 or 13% added ethanol.

TABLE 18 Solubility chart of treprostinil prodrugs in HFA-134a with added ethanol. HFA- 134a C₁₂-TR C₁₄-TR C₁₆-TR 5C₉-TR C₆-TR-A C₁₂-TR-A 13% S S R S n/e n/e EtOH 10% S S R R S S EtOH 7% S R R R R R EtOH 5% R R R R R R EtOH 3% R R n/e R R P EtOH S—soluble; R—thin liquid-vapor ring is visible; P—precipitate is visible; n/e—not evaluated.

TABLE 18 Solubility chart of treprostinil derivatives in HFA-227 with added ethanol. HFA-227 C₁₂-TR C₁₄-TR C₁₆-TR 5C₉-TR C₆-TR-A C₁₂-TR-A 13% S n/e S S n/e n/e EtOH 10% n/e R n/e n/e n/e S EtOH 7% n/e R R R R R EtOH 5% n/e n/e R n/e R R EtOH 3% R R n/e R R P EtOH S—soluble; R—thin liquid-vapor ring is visible; P—precipitate is visible; n/e—not evaluated.

Example 17 Pharmacokinetis of Blood Plasma Treprostinil After Inhalation of C₁₂ Amide Linked Treprostinil Nanoparttcle Formulation in Ventilated Rats

Male Sprague Dawley rats (N=3) were anesthetized and prepared with endotracheal tube for ventilation. The right femoral vein was cannulated to facilitate blood collections. Rats were administered the lipid nanoparticle formulation T763, which has the following components: (C₁₂-TR-A 45 mol %, squalane 45 mol %, DSPE-PEG2000 10 mol %).

Aeroneb® nebulizer and a controller (Aerogen, Dangan, Galway, Ireland) were used to produce aerosol of a mass median aerodynamic diameter (MMAD) between 2.5 μm and 4 μm and at a rate of 0.1 mL/min.

A SAR-830/AP Small Animal Ventilator (CWE Inc., Ardmore, Pa.) set up at ventilator tidal volume (VT) of 8 mL/kg, rate of 90 breaths/min was used to deliver nebulized test articles of volume 300 μL. The targeted dose was 6 ug/kg of Treprostinil equivalent.

The plasma level of treprostinil were significantly lower than when nanoparticle formulation T568 (C₁₂-TR 40 mol %, squalane 40 mol %, chol-PEG2k 10 mol %, DOPC 10 mol %), containing C₁₂-TR alkyl ester was used with the same dose. This suggests that the con version rate of the amide prodrug is much slower than the rate for the ester prodrug of treprostinil.

While the described invention has been described with reference to the specific embodiments thereof it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adopt a particular situation, material, composition of matter, process, process step or steps, to the objective spirit and scope of the described invention. All such modifications are intended to be within the scope of the claims appended hereto.

Patents, patent applications, patent application publications, journal articles and protocols referenced herein are incorporated by reference in their entireties, for all purposes. 

1.-180. (canceled)
 181. A method of treating pulmonary fibrosis in a patient in need thereof comprising administering to the patient a composition comprising an effective amount of a compound of Formula (II), or a pharmaceutically acceptable salt thereof,

wherein R₁ is O; R₂ is tetradecyl, pentadecyl, hexadecyl, heptadecyl or octadecyl and n is an integer from 0 to
 5. 182. The method of claim 181, wherein administering comprises pulmonary administration.
 183. The method of claim 181, wherein administering comprises oral, nasal, intravenous or subcutaneous administration.
 184. The method of claim 182, wherein pulmonary administration comprises administration via a metered dose inhaler, a dry powder inhaler or a nebulizer.
 185. The method of claim 181, wherein the effective amount of the compound of Formula (II), or the pharmaceutically acceptable salt thereof, is administered once daily.
 186. The method of claim 181, wherein the effective amount of the compound of Formula (II), or the pharmaceutically acceptable salt thereof, is administered two or more times daily.
 187. The method of claim 181, wherein n is
 1. 188. The method of claim 181, wherein R₂ is hexadecyl.
 189. The method of claim 188, wherein n is
 1. 190. The method of claim 182, wherein n is 1, R₂ is hexadecyl and pulmonary administration comprises administration via a nebulizer.
 191. The method of claim 190, wherein the nebulizer is a vibrating mesh nebulizer.
 192. The method of claim 182, wherein n is 1, R₂ is hexadecyl and pulmonary administration comprises administration via a dry powder inhaler.
 193. The method of claim 181, wherein the composition further comprises a lipid-polyethylene glycol (PEG) conjugate.
 194. The method of claim 193, wherein the PEG is PEG-400, PEG500, PEG 1000, PEG2000, PEG3000, PEG4000 or PEG5000.
 195. The method of claim 193, wherein the PEG is PEG2000.
 196. The method of claim 193, wherein the lipid is cholesterol.
 197. The method of claim 193, wherein the lipid is a phospholipid.
 198. The method of claim 193, wherein the lipid is phosphatidylethanoiarnine (DSPE), dimyristoyl phosphoethanol amine (DMPE) or distearoyl glycerol (DSG).
 199. The method of claim 193, wherein the lipid-PEG conjugate is cholesterol-PEG2000, DSPE-PEG 1000 or DSG-PEG2000.
 200. The method of claim 181, wherein the composition further comprises a hydrophobic additive.
 201. The method of claim 200, wherein the hydrophobic additive is a hydrocarbon, a terpene or a hydrophobic lipid, alkyl ester, cholesteryl ester or an alkyl-glyceride.
 202. The method of claim 200, wherein the hydrophobic additive is a terpene.
 203. The method of claim 202, wherein the terpene is squalane.
 204. The method of claim 189, wherein the composition further comprises a lipid-polyethylene glycol (PEG) conjugate.
 205. The method of claim 204, wherein the PEG is PEG400, PEG500, PEG 1000, PEG2000, PEG3000, PEG4000 or PEG-5000.
 206. The method of claim 204, wherein the PEG is PEG-2000.
 207. The method of claim 205, wherein the lipid is cholesterol.
 208. The method of claim 205, wherein the lipid is a phospholipid.
 209. The method of claim 205, wherein the lipid is phosphatidylethanolamine (DSPE), dimyristoyl phosphoethanolamine (DMPE) or distearoyl glycerol (DSG).
 210. The method of claim 204, wherein the lipid-PEG conjugate is cholesterol—PEG2000, DSPE-PEG 1000 or DSG-PEG2000.
 211. The method of claim 210, wherein the composition further comprises a hydrophobic additive.
 212. The method of claim 211, wherein the hydrophobic additive is a terpene.
 213. The method of claim 212, wherein the terpene is squalane. 